Methods and compositions for achieving hemostasis and stable blood clot formation

ABSTRACT

Provided is a tunable biopolymer hydrogel produced from two processed natural polysaccharides for use as a hemostat. If desired, the hydrogel formation can be tuned so that the hydrogel forms within seconds when applied to a tissue lesion. The resulting hydrogel can adhere to tissue and, without swelling, produce hemostasis within seconds after application to tissue of interest. The hydrogel also captures, aggregates and concentrates platelets and red blood cells at the site of the tissue lesion thereby initiating a clotting cascade at the site of the lesion. The hemostat can be used to prevent blood loss during surgical procedures, for example, during brain, spine or other surgical procedures where hemostasis is desirable, and is particularly useful during surgical procedures where swelling of the hemostat (e.g., in the brain or spine) would be detrimental to the subject.

CROSS-REFERENCE

This application claims the benefit of, and priority to, U.S. Provisional Application No. 62/769,161, filed Nov. 19, 2018, the content of which is hereby incorporated by reference in its entirety.

FIELD

The invention relates generally to methods and compositions for achieving hemostasis and blood coagulation, and more specifically relates to methods and compositions for achieving hemostasis and blood coagulation during surgical procedures.

BACKGROUND

Bleeding and blood loss are problems that must be addressed during and at the conclusion of surgery and other medical procedures. Significant blood loss can be fatal or cause significant morbidity, and surgeons and medical staff routinely compensate for blood loss with transfusions and the use of recirculating devices. A number of different techniques and products are currently used by surgeons to stop bleeding and effect hemostasis in surgery and medical procedures. However no single approach is effective or suitable under all circumstances, and the currently available approaches have limitations in effectiveness, safety, applicability and ease of use.

The most commonly used approaches involve closing a tissue or blood vessel mechanically with a suture or staple. This ligature technique is often effective, though it may allow for minor bleeding to occur around suture or staple holes. Sometimes biological or synthetic adhesives are applied to either complement or replace sutures or staples to stop this blood flow. However, tissue sealants are not hemostats per se and allow the pooling of blood underneath the seal in cases of moderate bleeding that may result in the formation of a hematoma. Hemostatic products which require time-consuming application or which produce slow effective action can be costly both in terms of financial costs due to greater operating room time and in terms of post procedure patient morbidity. Some techniques and products have limited effectiveness in certain applications, which may require a surgeon to reapply the product or switch to another product, which can be both time consuming and costly.

Under certain circumstances standard ligature techniques are inappropriate or not feasible. In such cases, an absorbable hemostatic product can be applied to the bleeding surface with a goal of achieving hemostasis that will later lead to a durable clot formation. Passive hemostats can control bleeding through absorption and may be powders, gauze, sponges or cross-linked gelatin. Sometimes these are augmented with an active hemostatic agent such as thrombin to try to achieve a successful hemostasis. However, the efficacy of these products is often variable and their use has been associated with adverse effects which can provide significant challenges during a surgical procedure. Such challenges become especially pronounced in certain surgical procedures such as brain and spinal surgeries. For example, certain sponges derived from porcine material can absorb up to 45-times their weight in blood and fluids resulting in significant swelling of the product that can lead to a patient experiencing adverse reactions such as pain, paresis or paralysis that can require revision surgery to address. Certain particulate hemostats have been reported to have caused cerebral edema. Gelatin-based devices typically swell during use and have been reported to cause mass effects leading to the development and progression of hemiparesis that required revision surgery to address the situation. Other adverse events and complications have been reported for all these types of hemostats. Most of these devices rely on absorption of blood and body fluids to produce hemostasis, which results in swelling and can lead to the reported mass effects.

The slow action of available absorbable hemostats, which are often used multiple times per case, can add to the length of surgical procedures, adding to expense and post-operative morbidity. Certain commercially available hemostats require as much as 10 minutes to produce hemostasis for each incidence of bleeding during a surgical procedure.

Accordingly, there remains a need for a fast acting, ready to use, biocompatible, biodegradable hemostat that minimizes or prevents bleeding and blood loss, does not swell during use and promotes stable clot formation during a wide variety of surgical procedures including cranial and spinal surgeries and in minimally invasive surgical procedures, and significantly reduces the incidence of postoperative adverse events.

SUMMARY OF THE INVENTION

The invention is based upon the discovery that it is possible to create a fast-acting biocompatible hemostat that promotes coagulation, produces hemostasis, does not swell during use, is adherent and does not migrate away from a site of application, is transparent, and is biodegradable.

The invention provides a “tunable” biopolymer system that addresses heretofore unmet needs in the field of hemostasis. In this system, two processed natural polysaccharides in the form of separate solutions are simultaneously mixed and applied onto a bleeding site, where they form a hydrogel device in situ. The hydrogel can form and produces hemostasis within seconds after application. The system may also be designed or “tuned” to produce hydrogels and facilitate hemostasis more slowly depending on the specific method of use. Rapid hemostasis can also contribute to the reduction of major complications in some surgical procedures by facilitating a shorter procedure time. It is believed that the rapid hemostasis acts to quickly stop bleeding and the hydrogel comprises specific intrinsic properties resulting in the simultaneous capture, aggregation and concentration of platelets and red blood cells to initiate the cascade of coagulation, which is accomplished without the use of exogenously added clotting agents, drugs or other chemicals. The resulting hemostatic action assures that the device does not act simply as a tamponade or sealant that might allow the pooling of blood and formation of a hematoma under a sealant.

The hydrogel itself forms without the use of a third chemical or synthetic cross-linking agent and thus avoids the potential for irritation and cytotoxicity or the interference with predictable rapid biodegradation associated with cross-linking agents. Furthermore, due to the internal chemistry, the hydrogel itself gently and predictably contracts over time and does not swell, even when immersed in blood or body fluids. This feature permits the hemostats described herein to be used in brain, spinal or other surgical procedures in which swelling of a hemostatic agent can lead to mass effects and subsequent complications, which themselves require medical or surgical intervention.

Furthermore, the hydrogel provided herein is essentially transparent, so that a surgeon can visually verify its action and effect in real time. This feature allows surgeons to proceed with the surgical procedure and close the site while verifying hemostasis, in contrast to hemostats which are opaque.

Furthermore, the hydrogel provided herein is cohesively strong and thus can quickly establish its initial tamponade effect. Furthermore, the hemostat is also adherent and does not migrate away from the application site. The hydrogel forms in intimate continuous contact with the bleeding site so that all sources of bleeding are exposed and treated to the hemostatic action of the device.

The hemostatic hydrogel is produced by combining a defined acrylated chitosan composition as described herein to a defined oxidized dextran composition also described herein to produce a hemostatic hydrogel having the structural and/or functional properties discussed herein. The characteristics of the acrylated chitosan and oxidized dextran together with their respective syntheses required to produce a hemostatic hydrogel having the desired properties are discussed below.

In one aspect, the invention provides an acrylated chitosan composition for use in creating the hemostat described herein, wherein the acrylated chitosan composition comprises acrylated chitosan comprising:

(i) from about 0.01 to about 0.3 mole fraction of a first monomer of formula (I)

(ii) from about 0.3 to about 0.75 mole fraction of a second monomer of formula (II)

and

(iii) from about 0.2 to about 0.7 mole fraction of a third monomer of formula (III)

In certain embodiments, the acrylated chitosan composition comprises (i) from about 0.01 to about 0.26 mole fraction of the first monomer of formula (I), (ii) from about 0.35 to about 0.65 mole fraction of the second monomer of formula (II), (iii) from about 0.3 to about 0.6 mole fraction of the third monomer of formula (III), or a combination of (i) and (ii), (i) and (iii), (ii) and (iii), and (i), (ii) and (iii). In certain embodiments, the acrylated chitosan comprises less than about 0.1 mole fraction of a fourth monomer of formula (IV)

In each of the foregoing, the acrylated chitosan can have (i) a weight-average molecular weight (Mw) of from about 25 kDa to about 400 kDa or from about 115 kDa to about 200 kDa, (ii) a number-average molecular weight (Mn) of from about 14 kDa to about 200 kDa or from about 55 kDa to about 140 kDa, (iii) a polydispersity index (PDI) of from about 1.5 (Mw/Mn) to about 3.5 (Mw/Mn), (iv) a PDI of from about 1.5 (Mz/Mw) to about 7.0 (Mz/Mw), or from about 1.6 (Mz/Mw) to about 3.0 (Mz/Mw) or a combination of two, three or four of each of the foregoing features.

In certain embodiments, the acrylated chitosan composition comprises from about 1% (w/w) to about 25% (w/w), or from about 1% (w/w) to about 10% (w/w). In other embodiments, the acrylated chitosan composition has a viscosity of from about 10 cP to about 50,000 cP, or from about 100 cP to about 25,000 cP.

In another aspect, the invention provides a method of preparing an acrylated chitosan composition (for example, the acrylated chitosan compositions described above) comprising the steps of (a) contacting a raw chitosan material with an aqueous organic acid solution (e.g., a 1% (v/v) aqueous organic acid solution) to form a chitosan intermediate; (b) contacting the chitosan intermediate with an α,β-unsaturated carboxylic acid (e.g., acrylic acid) to form an acrylated chitosan intermediate; and (c) purifying the acrylated chitosan intermediate to produce an acrylated chitosan composition of the present invention.

In certain embodiments, during step (a), the step of contacting the raw chitosan material with the aqueous organic acid solution is conducted at (i) a pressure of about 2 atmospheres, (ii) a temperature from about 80° C. to about 120° C., or a combination thereof. In certain embodiments, during step (a), (i) the PDI (Mw/Mn) of the chitosan intermediate is from about 15% to about 40% less than the PDI (Mw/Mn) of the raw chitosan material, (ii) the raw chitosan material has a PDI of from about 1.5 (Mw/Mn) to about 5.0 (Mw/Mn), (iii) the raw chitosan material has a degree of deacetylation of from about 65% to about 99% or from about 70% to about 98%, or a combination of (i) and (ii), (i) and (iii), (ii) and (iii), and (i), (ii) and (iii).

In certain embodiments, the during step (b), (i) the chitosan intermediate is contacted with the α,β-unsaturated carboxylic acid at a temperature from about 50° C. to about 120° C., (ii) the acrylated chitosan intermediate has a degree of substitution (DS) value of from about 25% to about 65%, or a combination of (i) and (ii). In certain embodiments, the method further comprises the step of precipitating the acrylated chitosan composition to provide a solid and then optionally or in addition dissolving the solid into an aqueous medium to form a solution comprising an amount of the acrylated chitosan composition. In certain embodiments, the acrylated chitosan composition comprises from about 1% to about 25%, or from about 1% to about 10% of the acrylated chitosan by weight of the total weight of the solution.

In another embodiment, the invention provides a method of preparing an acrylated chitosan composition comprising the steps of: (a) contacting a raw chitosan material with an acetic acid solution to form a chitosan intermediate, wherein the raw chitosan material has a PDI of from about 1.5 (Mw/Mn) to about 5.0 (Mw/Mn); (b) contacting the intermediate chitosan with acrylic acid to form an acrylated chitosan intermediate having a degree of substitution (DS) value of from about 25% to about 65%; and (c) purifying the acrylated chitosan intermediate to produce an acrylated chitosan composition of the present invention. The method may further comprise the step of precipitating the acrylated chitosan composition produced in step (c) to provide a solid and then optionally or in addition dissolving the solid into an aqueous medium to form a solution comprising from about 1% to about 10% acrylated chitosan composition (w/w) by weight of the total weight of the solution.

In another aspect, the invention provides an oxidized dextran composition for use in creating the hemostat described herein, wherein the oxidized dextran composition comprises oxidized dextran comprising:

-   -   (a) less than about 0.8 mole fraction of a first monomer of         formula (V)

-   -    and     -   (b) from about 0.1 to about 1.0 mole fraction of a second         monomer, wherein the second monomer is selected from a monomer         of formula (VI), a monomer of formula (VII) and a combination of         formula (VI) and formula (VII)

In certain embodiments, the oxidized dextran composition comprises (i) from about 0.4 to about 0.7 mole fraction of the first monomer of formula (V), (ii) from about 0.15 to about 0.35 mole fraction of the second monomer, (iii) comprises less than about 0.65 mole fraction of a third monomer of formula (VIII)

or a combination of (i) and (ii), (i) and (iii), (ii) and (iii), or (i), (ii) and (iii).

In certain embodiments, the oxidized dextran has (i) a Mw of from about 10 kDa to about 300 kDa or from about 15 kDa to about 90 kDa, (ii) a Mn of from about 4 kDa to about 166 kDa or from about 4 kDa to about 45 kDa, (iii) a PDI of from about 1.8 (Mw/Mn) to about 6.0 (Mw/Mn) or from about 2.0 (Mw/Mn) to about 4.0 (Mw/Mn), (iv) a PDI of from about 1.5 (Mz/Mw) to about 6.0 (Mz/Mw) or from about 1.5 (Mz/Mw) to about 5.0 (Mz/Mw), or a combination of any of the foregoing features.

In certain embodiments, the oxidized dextran comprises a total amount of aldehyde groups of from about 0.5 to about 2.0 or from about 0.6 to about 0.9 mol aldehydes/mol oxidized dextran. In other embodiments, the oxidized dextran contains a ratio of primary aldehyde groups to secondary aldehyde groups from about 1.5 to about 6.0 or from about 1.8 to about 3.5. In certain other embodiments, the oxidized dextran composition has a degree of oxidation from about 25% to about 100% or from about 30% to about 50%. In certain other embodiments, the oxidized dextran composition comprises from about 1% (w/w) to about 25% (w/w), or from about 1% (w/w) to about 10% (w/w) of the oxidized dextran. In certain other embodiments, the oxidized dextran composition has a viscosity of from about 1 cP to about 2,000 cP, from about 1 cP to about 100 cP, or from about 1 cP to about 10 cP.

In another aspect, the invention provides a method of preparing an oxidized dextran composition (for example, any of the oxidized dextran compositions described herein), the method comprising the steps of: (a) contacting a solution comprising a dextran material (for example, a raw dextran material) with an oxidizing agent to form an oxidized dextran intermediate, wherein the concentration of the dextran material in the solution is greater than 1% (w/w) (for example, 1.1%, 1.2%, 1.3%, etc.); and (b) purifying the oxidized dextran intermediate to produce an oxidized dextran composition.

In certain embodiments, the oxidized dextran composition produced in step (b) is the oxidized dextran composition described herein and used to produce the hemostatic hydrogels described herein.

In certain embodiments, the raw dextran material has (i) a Mw of from about 50 kDa to about 2,000 kDa, (ii) a PDI of from about 1.4 (Mw/Mn) to about 5.0 (Mw/Mn), or a combination of (i) and (ii). In certain embodiments, the oxidizing agent is a periodate salt. In certain embodiments, the method comprises the additional step of precipitating the oxidized dextran composition to provide a solid and then optionally or in addition comprises the step of dissolving the solid into an aqueous medium to form a solution comprising an amount of the oxidized dextran composition. In certain embodiments, the amount of the oxidized dextran composition in the solution is from about 1% (w/w) to about 25% (w/w), or from about 1% (w/w) to about 10% (w/w) by weight of the total weight of the solution.

In another aspect, the invention provides a hemostatic hydrogel composition containing oxidized dextran and acrylated chitosan, wherein the hydrogel composition has two or more of the following features:

-   -   (i) the hydrogel composition comprises a total amount of free         aldehyde groups of from about 0.1 to about 0.7 moles         aldehyde/mole oxidized dextran,     -   (ii) the hydrogel composition is formed from oxidized dextran         and acrylated chitosan, wherein the ratio of primary aldehydes         in the oxidized dextran to the amines in the acrylated chitosan         is in the range from about 1.0 to about 2.0, and/or the ratio of         total aldehydes in the oxidized dextran to amines in the         acrylated chitosan is from about 1.5 to about 3.0,     -   (iii) the ratio of Mw of the acrylated chitosan to the oxidized         dextran is from about 2 to about 10, the ratio of Mn of the         acrylated chitosan to the oxidized dextran is from about 4 to         about 15, the ratio of Mz of the acrylated chitosan to the         oxidized dextran is from about 2 to about 10, the ratio of PDI         (Mw/Mn) of acrylated chitosan to oxidized dextran is from about         0.5 to about 0.8, and/or the ratio of PDI (Mz/Mw) of acrylated         chitosan to oxidized dextran is from about 0.5 to about 1.0,     -   (iv) upon formation of the hydrogel composition, the hydrogel         composition comprises a bound water content of from about 65%         w/w to about 95% w/w,     -   (v) the hydrogel composition comprises a three-dimensional         porous structure comprising layers of substantially         non-interconnected pores having (a) a pore size distribution         from about 10 μm to about 850 μm in diameter, (b) a platelet         adhesive surface, or a combination of (a) and (b),     -   (vi) the hydrogel composition comprises walls disposed between         the substantially non-interconnected pores, the walls having a         wall thickness of from 0.046 μm to 50 μm,     -   (vii) the hydrogel composition comprises pores certain of which         define a platelet adhesive surface so that, when in contact with         blood, the hydrogel composition permits platelets and/or red         blood cells within the blood to adhere to the platelet adhesive         surface and promote blood clot formation at or within the         hydrogel composition,     -   (viii) the hydrogel composition comprises pores certain of which         define a platelet adhesive surface so that, when in contact with         blood, the hydrogel composition permits platelets and/or red         blood cells within the blood to adhere to the platelet adhesive         surface and not permit platelets and/or red blood cells from the         blood to enter pores present in a first surface of the hydrogel         composition, pass through the hydrogel composition, and then         exit the hydrogel composition via pores present in a second         surface of the hydrogel composition that opposes the first         surface,     -   (ix) at about 10 seconds after the formation of the hydrogel         composition, the hydrogel composition has a burst strength of         greater than 20 mmHg as determined using an ASTM F 2392-04         protocol,     -   (x) at about 2 minutes after the formation of the hydrogel         composition, the hydrogel composition has a burst strength of         greater than about 35 mmHg as determined using an ASTM F 2392-04         protocol,     -   (xi) at about 5 minutes after the formation of the hydrogel         composition, the hydrogel composition has a burst strength of         greater than about 70 mmHg as determined using an ASTM F 2392-04         protocol,     -   (xii) the hydrogel composition has an elastic modulus of from         about 500 Pa to about 5000 Pa at from about 10 seconds to about         80 seconds after the formation of the hydrogel composition,     -   (xiii) the hydrogel composition has a compression modulus of         from about 3 kPa to about 250 kPa,     -   (xiv) the hydrogel composition has an average adhesion strength         of from about 1.0 N to about 50 N, as determined using an ASTM F         2258-05 protocol,     -   (xv) the volume of the hydrogel composition, when formed, does         not increase upon exposure to a physiological fluid or body         fluid,     -   (xvi) the hemostatic hydrogel composition shrinks from about 5%         to about 30% within about 2 hours after formation, from about         20% to about 60% within about 8 hours after formation, and from         about 45% to about 70% within about 24 hours after formation,         when exposed to a temperature of 37° C. and 75% relative         humidity,     -   (xvii) the volume of the hydrogel composition shrinks by less         than about 5% about 10 minutes after formation when exposed to a         physiological fluid or body fluid,     -   (xviii) the hydrogel composition is substantially transparent         when the hydrogel composition has a thickness of 2 mm to 10 mm,         and     -   (xix) the hydrogel composition optionally further comprises a         therapeutic agent.

In certain embodiments, the hemostatic hydrogel composition comprises a gel produced by combining oxidized dextran with an acrylated chitosan composition produced by dissolving chitosan in an organic acid prior to acrylation. In certain embodiments, the organic acid is acetic acid.

In certain embodiments, the hemostatic hydrogel comprises a plurality of crosslinked moieties of formula (IX)

In another aspect, the invention provides a hemostatic hydrogel composition comprising a gel produced by combining oxidized dextran with acrylated chitosan, wherein the hemostatic hydrogel composition comprises a plurality of crosslinked moieties of formula (IX)

and further comprises one or more of the following features:

-   -   (i) the hemostatic hydrogel, when immersed in saline for about 4         hours exhibits a mass reduction of at least 1%, for example from         about 1% to about 5%,     -   (ii) the hemostatic hydrogel, when immersed in saline for about         8 hours exhibits a mass reduction of at least 6%, for example         from about 6% to about 10%,     -   (iii) the hemostatic hydrogel, when immersed in saline for about         24 hours exhibits a mass reduction of at least 20%, for example         from about 20% to about 25%,     -   (iv) the hemostatic hydrogel, when exposed to a physiological         fluid or body fluid for about 8 hours exhibits an irreversible         decrease in volume, and     -   (v) the hemostatic hydrogel, at least 30 seconds after         formation, takes at least 5 minutes to completely dissolve when         exposed to a 5M hydroxylamine hydrochloride solution.

In certain embodiments, the hemostatic hydrogel exhibits an increase in density at 4 hours after being immersed in the saline solution relative to the hydrogel prior to immersion. In certain embodiments, the hemostatic hydrogel permits Schiff base rearrangement thereby increasing the density of the crosslinked moieties of formula (IX). In certain embodiments, the number of crosslinked moieties of formula (IX) increases for at least about 24 hours after the formation of the hemostatic hydrogel composition. In certain embodiments, the density of crosslinked moieties of formula (IX) increases for at least about 24 hours after the formation of the hemostatic hydrogel composition.

In certain embodiments, the hemostatic hydrogel composition comprises:

(a) from about 0.0 to about 0.3 mole fraction of a first monomer of formula (I)

(b) from about 0.02 to about 0.7 mole fraction of a second monomer of formula (III),

and

(c) from about 0.0 to about 0.8 mole fraction of a third monomer of formula (V),

In certain embodiments, the hemostatic hydrogel composition comprises (i) from about 0.0 to about 0.26 mole fraction of the first monomer of formula (I), (ii) from about 0.03 to about 0.6 mole fraction of the second monomer of formula (III), (iii) from about 0.04 to about 0.7 mole fraction of the third monomer of formula (V), or a combination or (i) and (ii), (i) and (iii), (ii) and (iii) and (i), (ii) and (iii).

In certain embodiments, the hemostatic hydrogel composition comprises (i) no greater than about 0.2 mole fraction of a fourth monomer of formula (IV)

(ii) no greater than about 0.65 mole fraction of a fifth monomer of formula (VIII)

or a combination or (i) and (ii).

In another aspect, the invention provides a method of preparing a hemostatic hydrogel composition (such as the hemostatic hydrogel compositions described herein), the method comprising contacting an acrylated chitosan composition as described herein with an oxidized dextran composition as described herein so as to form the hemostatic hydrogel composition.

In certain embodiments, the ratio of the viscosity of the acrylated chitosan composition to the oxidized dextran composition ranges from about 100:1 to about 10,000:1. In certain embodiments, the hemostatic agent further comprises a therapeutic agent or a cell, for example, a stem cell.

In certain embodiments, the hemostatic hydrogel is produced by contacting the acrylated chitosan composition described herein with the oxidized dextran composition described herein in a static mixer and optionally or in addition then aerosolizing the mixture prior to application to tissue. In certain embodiments, the gelation time of the hemostatic hydrogel composition is less than 30 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition. However, depending upon the circumstances, for example, the desired application, the gelation time of the hemostatic hydrogel composition can be tuned to be within from about 10 seconds to about 240 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition.

In another aspect, the invention provides a method of promoting hemostasis (e.g., reducing or stopping blood loss) at a location in a subject in need thereof. The method comprises forming at the location in the subject the hemostatic hydrogel composition described herein thereby to promote hemostasis (e.g., reduce or stop blood loss) at the location. It is understood that the hemostatic hydrogel composition adheres to a tissue surface at the location. Furthermore, it is understood that the hydrogel permits the platelets and/or red blood cells to adhere to or otherwise become disposed on the surfaces of pores in the hemostatic hydrogel and promote a blood coagulation cascade at the location thereby to produce a blood clot. It is understood that blood loss at the location can be caused by, for example, trauma, abrasion, or surgical intervention at the location.

The hemostatic hydrogel composition, when applied to the location, can fill a cavity at the location without inducing compression of tissue surrounding the cavity when the hemostatic hydrogel composition is exposed to physiological fluid or a body fluid. It is understood that hemostasis can be achieved from about 5 seconds to about 120 seconds, from about 10 seconds to about 120 seconds, from about 15 seconds to about 120 seconds, from about 5 seconds to about 60 seconds, from about 10 seconds to about 60 seconds, from about 15 seconds to about 60 seconds, from about 5 seconds to about 30 seconds, from about 10 seconds to about 30 seconds, from about 10 seconds to about 20 seconds, from about 15 seconds to about 30 seconds, from about 15 seconds to about 20 seconds, from about 5 seconds to about 20 seconds, from about 5 seconds to about 15 seconds, or from about 10 seconds to about 15 seconds, after the hemostatic hydrogel composition is applied to the location.

In certain embodiments, the method further comprises removing the hemostatic hydrogel composition from the subject after hemostasis. In certain embodiments, the hemostatic hydrogel composition is removed by exposing the hemostatic hydrogel composition to a dissolution agent that dissolves the hemostat. In certain embodiments, the dissolution agent is an organic compound comprising a primary amine and capable of breaking Schiff base linkages.

In another aspect, the invention provides a method of achieving hemostasis at a location in a subject in need thereof. The method comprises forming at the location in the subject the hemostatic hydrogel composition described herein to facilitate hemostasis and removing the hemostatic hydrogel composition from the subject after hemostasis.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a scanning election microscope (SEM) image of the internal three-dimensional structure of an exemplary acrylated chitosan/oxidized dextran hydrogel.

FIG. 2 is a SEM image of the surface of an exemplary acrylated chitosan/oxidized dextran hydrogel.

FIG. 3 is a graph showing the elastic modulus of an exemplary acrylated chitosan/oxidized dextran hydrogel as a function of time.

FIG. 4 is a graph showing the elastic storage modulus and the viscous loss modulus of an exemplary 2% (w/w) acrylated chitosan/2% (w/w) oxidized dextran hydrogel as a function of time.

FIG. 5 is a graph showing the elastic storage modulus and the viscous loss modulus of an exemplary 7% (w/w) acrylated chitosan/7% (w/w) oxidized dextran hydrogel as a function of time.

FIG. 6 is a graph showing the weight of an exemplary acrylated chitosan/oxidized dextran hydrogel following formation of a hydrogel as a function of time.

FIG. 7 is a graph showing the diameter of an exemplary acrylated chitosan/oxidized dextran hydrogel exposed to moisture at room temperature following formation of a hydrogel as a function of time.

FIG. 8 is a graph showing the weight of exemplary acrylated chitosan/oxidized dextran hydrogels immersed in saline solution following formation of a hydrogel as a function of time.

FIG. 9 shows SEM images of (a) an exemplary acrylated chitosan/oxidized dextran hydrogel after formation and (b) an exemplary acrylated chitosan/oxidized dextran hydrogel immersed in saline solution for about 100 days.

FIG. 10 is an overlay of pore size distribution data of an exemplary acrylated chitosan/oxidized dextran hydrogels after formation and an exemplary acrylated chitosan/oxidized dextran hydrogels after immersion in saline solution for about 100 days.

FIG. 11 is a graph showing the percentage of shrinkage of exemplary acrylated chitosan/oxidized dextran hydrogels comprising 0.85% NaCl, 33% NaCl and 33% CaCl₂ following formation of a hydrogel as a function of time.

FIG. 12 is an SEM image of a blood clot formed within a pore of an exemplary acrylated chitosan/oxidized dextran hydrogel following formation of a hydrogel at an abrasion wound on a porcine liver.

FIG. 13 is an SEM image of a blood clot formed within a pore of an exemplary acrylated chitosan/oxidized dextran hydrogel following formation of a hydrogel at a punch biopsy wound on a porcine liver.

FIG. 14 is an SEM image of a blood clot formed within a pore of an acrylated chitosan/oxidized dextran hydrogel following formation of a hydrogel at a laceration on a porcine liver.

FIG. 15 is an SEM image of a blood clot formed on an acrylated chitosan/oxidized dextran hydrogel following formation of a hydrogel at a laceration on a porcine spleen.

FIG. 16 is an overlay of SEC-MALS spectra of an acrylated chitosan composition prepared using the method described in U.S. Pat. No. 7,854,923 (Ac(A)) and an exemplary acrylated chitosan composition described herein (Ac(B)).

FIG. 17 is an overlay of dissolution rate data for an exemplary hemostatic hydrogel composition (EDM hydrogel) and a hemostatic hydrogel composition prepared using the method described in U.S. Pat. No. 7,854,923 ('923 hydrogel) dissolved in 5M aqueous hydroxylamine hydrochloride solutions.

FIG. 18 is a graph showing the time to complete dissolution for an exemplary hemostatic hydrogel composition, prepared using 7% (w/w) acrylated chitosan and oxidized dextran compositions, dissolved in 5M aqueous hydroxylamine hydrochloride solutions.

DETAILED DESCRIPTION OF THE INVENTION I Definitions

To facilitate an understanding of the present invention, a number of terms and phrases are defined below.

The terms “a” and “an” as used herein mean “one or more” and include the plural unless the context is inappropriate.

As used herein, the term “tissue” refers to material that forms the solid or semi-solid structures that make up any of the organs or components of a living organism and includes, for example, membrane, skin, muscle, bone, cartilage, nerve and nerve sheathe, meninge, connective tissue, blood vessel, the sclera or iris of the eye, the solid materials constituting internal organs such as liver, stomach, pancreas, intestine, kidney, thymus, uterus, testes, bladder, lung, heart and any other internal structures that are solid or semi-solid in texture. Thus, liquids such as blood are not considered to be a tissue.

“Adhere” or “adherence” refers to the creation of a physical bond between material and tissue such that a moderate motion or force does not cause separation of the material from the tissue on which it is disposed. The physical bond that is created between the material and the tissue that requires hemostasis may have one or several bases including electrostatic bonding and covalent bonding, but any mechanism by which the adherence occurs is contemplated herein.

The terms “adhesive” and “adhesivity” similarly refer to the existence of a physical bond between two materials such as a hemostat of the present invention and the tissue to which the hemostat is applied. An adhesive is a material which adheres to tissue or other material and which may be used to constrain the separation of two tissue masses. Adhesivity is the property or degree to which a material adheres to a tissue or other material.

As used herein, the term “hydrogel” refers to a material of solid or semi-solid texture that comprises water. Hydrogels are formed by a three-dimensional network of molecular structures within which water, among other substances, may be retained. The three-dimensional molecular network may be held together by covalent chemical bonds, or by ionic bonds, or by any combination thereof.

The act of “gelation” refers to the formation of a gel, for example, a hydrogel.

A “saccharide” as used herein refers to a carbohydrate. The term “carbohydrate” includes the class of compounds commonly known as sugars, in addition to compounds that are chemically related to sugars. The term thus includes simple “monosaccharide” sugars, “disaccharide” sugars as well as polymeric “polysaccharides.” The term encompasses a group of compounds including sugars, starches, gums, cellulose and hemicelluloses. The term further encompasses sugar derivatives such as amino-sugars, for example, 2-amino-2-deoxyglucose, as well as their oligomers and polymers; sulfated sugars; and sugars with hydroxyl, amino, carboxyl and other groups.

As used herein, the term “chitosan” refers to a polysaccharide polymer, either obtained from a natural source such as chitin, or synthetically prepared. Chemically, chitosan is predominantly a polymer of β-1,4-linked 2-amino-2-deoxyglucose monomers. When prepared from a natural source, the usual natural source is chitin, a major constituent of the shells of arthropods (e.g., crabs, lobsters, and shrimp), mollusks, annelids, and cephalopods (e.g., squid). Other natural sources of chitin include plants (e.g., fungi and algae). Chitin is chemically a polymer comprising β-1,4-linked 2-acetamino-2-deoxyglucose monomers. After isolation of chitin from its natural source, it is treated to cause hydrolysis of the acetamido group without cleavage of the sugar-sugar bonds, typically through alkaline hydrolysis. Chitosan is not a single molecular entity, but rather comprises polymeric chains of various lengths.

As used herein, the term “raw chitosan material” refers to a chitosan preparation derived from chitin derived from arthropods (e.g., crabs, lobsters, and shrimp), mollusks, annelids, cephalopods (e.g., squid), or plants (e.g., fungi) that has been treated to cause hydrolysis of the acetamido groups without substantial cleavage of sugar-sugar bonds, for example, by alkaline hydrolysis.

As used herein, the term “alkylated chitosan” refers to a chitosan molecule in which a carbon containing moiety has been covalently bonded. The term “alkylated chitosan” comprises a large number of possible chemical structures that share a common feature that chemical bonds have been formed between the components of the chitosan molecules and at least one carbon atom in each of the molecules that are bonded to the chitosan. For example, alkylated chitosan includes the methylation of chitosan, in which bonds are formed between methyl radicals or groups and atoms within the chitosan molecule, such as nitrogen, oxygen or carbon atoms. Other carbon-containing groups may likewise be chemically bonded to chitosan molecules to produce an alkylated chitosan. Examples include poly(oxyalkylene)chitosan, wherein poly(oxyethylene), or polyethyleneglycol, chains are covalently bonded to the chitosan backbone, as well as acrylated chitosans, formed by alkylation of chitosan with acrylates.

As used herein, the term “acrylated chitosan” refers to an alkylated chitosan wherein one or more acrylate groups have been allowed to react with, and form chemical bonds to, the chitosan molecule. An acrylate is a molecule containing an α,β-unsaturated carbonyl group; thus, acrylic acid is prop-2-enoic acid. The acrylate may bond to the chitosan through a Michael addition of the chitosan nitrogen atoms with the acrylate.

As used herein, the term “degree of substitution” of a polymeric species refers to the ratio of the average number of substituent groups, for example an alkyl substituent, per monomeric unit of the polymer.

As used herein, the terms “swell”, “swells” or “swelling” refers to the increase in mass and/or volume of a material (e.g., a hemostatic hydrogel composition of the present invention), by greater than about 3%, 4%, or 5% of the material's original mass and/or volume following exposure to a physiological fluid, body fluid, or aqueous medium.

As used herein, the term “complete dissolution”, when used in relation to dissolution of a hydrogel, refers to the time at which a sample of hydrogel (including particles or fragments of the hydrogel) can no longer be visually detected within a visually transparent liquid solution.

As used herein, the term “aqueous medium” refers to a liquid medium composed largely, but not necessarily exclusively, of water. Other components may also be present, such as salts, co-solvents, buffers, stabilizers, dispersants, colorants and the like.

As used herein, the terms “subject” and “patient” refer to organisms to be treated by the methods and/or compositions described herein. Such organisms are preferably mammals (e.g., murines, simians, equines, bovines, porcines, canines, felines, and the like), and more preferably humans.

As used herein, the term “effective amount” refers to the amount of a compound (e.g., a compound of the present invention) sufficient to effect beneficial or desired results. An effective amount can be administered in one or more administrations, applications or dosages and is not intended to be limited to a particular formulation or administration route. As used herein, the terms “treat,” “treating,” and “treatment” include any effect, e.g., lessening, reducing, modulating, ameliorating or eliminating, that results in the improvement of the condition, disease, disorder, and the like, or ameliorating a symptom thereof.

The phrase “therapeutically-effective amount” as used herein means that amount of a compound, material, or composition comprising a compound of the present invention which is effective for producing some desired therapeutic effect in a subject.

In the application, where an element or component is said to be included in and/or selected from a list of recited elements or components, it should be understood that the element or component can be any one of the recited elements or components, or the element or component can be selected from a group consisting of two or more of the recited elements or components.

Further, it should be understood that elements and/or features of a composition or a method described herein can be combined in a variety of ways without departing from the spirit and scope of the present invention, whether explicit or implicit herein. For example, where reference is made to a particular compound, that compound can be used in various embodiments of compositions of the present invention and/or in methods of the present invention, unless otherwise understood from the context. In other words, within this application, embodiments have been described and depicted in a way that enables a clear and concise application to be written and drawn, but it is intended and will be appreciated that embodiments may be variously combined or separated without parting from the present teachings and invention(s). For example, it will be appreciated that all features described and depicted herein can be applicable to all aspects of the invention(s) described and depicted herein.

It should be understood that the expression “at least one of” includes individually each of the recited objects after the expression and the various combinations of two or more of the recited objects unless otherwise understood from the context and use. The expression “and/or” in connection with three or more recited objects should be understood to have the same meaning unless otherwise understood from the context.

The use of the term “include,” “includes,” “including,” “have,” “has,” “having,” “contain,” “contains,” or “containing,” including grammatical equivalents thereof, should be understood generally as open-ended and non-limiting, for example, not excluding additional unrecited elements or steps, unless otherwise specifically stated or understood from the context.

Where the use of the term “about” is before a quantitative value, the present invention also includes the specific quantitative value itself, unless specifically stated otherwise. As used herein, the term “about” refers to a ±10% variation from the nominal value unless otherwise indicated or inferred.

It should be understood that the order of steps or order for performing certain actions is immaterial so long as the present invention remain operable. Moreover, two or more steps or actions may be conducted simultaneously.

The use of any and all examples, or exemplary language herein, for example, “such as” or “including,” is intended merely to illustrate better the present invention and does not pose a limitation on the scope of the invention unless claimed. No language in the specification should be construed as indicating any non-claimed element as essential to the practice of the present invention.

Throughout the description, where compositions and kits are described as having, including, or comprising specific components, or where processes and methods are described as having, including, or comprising specific steps, it is contemplated that, additionally, there are compositions and kits of the present invention that consist essentially of, or consist of, the recited components, and that there are processes and methods according to the present invention that consist essentially of, or consist of, the recited processing steps.

As a general matter, compositions specifying a percentage are by weight unless otherwise specified. Further, if a variable is not accompanied by a definition, then the previous definition of the variable controls.

The following sections describe the synthesis of acrylated chitosan and oxidized dextran which are used to form the hemostatic hydrogel compositions described herein.

II Acrylated Chitosan

In one aspect, the invention provides acrylated chitosan useful in producing the hemostatic hydrogel compositions described herein. In certain embodiments, the acrylated chitosan compositions comprise acrylated chitosan comprising:

(i) from about 0.01 to about 0.3 mole fraction of a first monomer of formula (I)

(ii) from about 0.3 to about 0.75 mole fraction of a second monomer of formula (II)

and

(iii) from about 0.2 to about 0.7 mole fraction of a third monomer of formula (III)

The term mole fraction, as used herein, refers to the mole fraction of a monomer present in a polymer and/or hydrogel composition disclosed herein, as determined without including the contribution of solvent (e.g., water) in the polymer and/or hydrogel composition.

In certain embodiments, the acrylated chitosan comprises from about 0.01 to about 0.26, from about 0.02 to about 0.26, from about 0.03 to about 0.26, from about 0.04 to about 0.26, from about 0.05 to about 0.26, from about 0.06 to about 0.26, from about 0.02 to about 0.23, from about 0.02 to about 0.19, from about 0.02 to about 0.16, from about 0.02 to about 0.13, from about 0.02 to about 0.1, from about 0.02 to about 0.07, from about 0.02 to about 0.04, from about 0.03 to about 0.23, from about 0.03 to about 0.19, from about 0.03 to about 0.16, from about 0.03 to about 0.13, from about 0.03 to about 0.1, from about 0.03 to about 0.07, from about 0.03 to about 0.04, from about 0.04 to about 0.23, from about 0.04 to about 0.19, from about 0.04 to about 0.16, from about 0.04 to about 0.13, from about 0.04 to about 0.1, from about 0.04 to about 0.07, from about 0.05 to about 0.23, from about 0.05 to about 0.19, from about 0.05 to about 0.16, from about 0.05 to about 0.13, from about 0.05 to about 0.1, from about 0.05 to about 0.07, from about 0.06 to about 0.23, from about 0.06 to about 0.19, from about 0.06 to about 0.16, from about 0.06 to about 0.13, from about 0.06 to about 0.1, or from about 0.06 to about 0.07 mole fraction of the first monomer of formula (I). In certain embodiments, the acrylated chitosan comprises from about 0.01 to about 0.26 mole fraction of the first monomer of formula (I). In certain embodiments, the acrylated chitosan comprises from about 0.02 to about 0.04, about 0.04 to about 0.07, or about 0.06 to about 0.16 mole fraction of the first monomer of formula (I).

In certain embodiments, the acrylated chitosan comprises from about 0.35 to about 0.65, from about 0.4 to about 0.65, from about 0.45 to about 0.65, from about 0.5 to about 0.65, from about 0.55 to about 0.65, from about 0.6 to about 0.65, from about 0.35 to about 0.6, from about 0.35 to about 0.6, from about 0.35 to about 0.55, from about 0.35 to about 0.5, from about 0.35 to about 0.45, from about 0.35 to about 0.4, from about 0.4 to about 0.6, from about 0.4 to about 0.55, from about 0.4 to about 0.5, from about 0.4 to about 0.45, from about 0.45 to about 0.6, from about 0.45 to about 0.55, from about 0.45 to about 0.5, from about 0.5 to about 0.6, from about 0.5 to about 0.55, or from about 0.55 to about 0.6 mole fraction of the second monomer of formula (II). In certain embodiments, wherein the acrylated chitosan comprises from about 0.35 to about 0.65 mole fraction of the second monomer of formula (II). In certain embodiments, wherein the acrylated chitosan comprises from about 0.35 to about 0.5, from about 0.45 to about 0.55, from about 0.5 to about 0.6 mole fraction of the second monomer of formula (II).

In certain embodiments, the acrylated chitosan comprises from about 0.3 to about 0.6, from about 0.35 to about 0.6, from about 0.4 to about 0.6, from about 0.45 to about 0.6, from about 0.5 to about 0.6, from about 0.55 to about 0.6, from about 0.3 to about 0.55, from about 0.3 to about 0.5, from about 0.3 to about 0.45, from about 0.3 to about 0.4, from about 0.3 to about 0.35, from about 0.35 to about 0.55, from about 0.35 to about 0.5, from about 0.35 to about 0.45, from about 0.35 to about 0.4, from about 0.4 to about 0.55, from about 0.4 to about 0.5, from about 0.4 to about 0.45, from about 0.45 to about 0.55, from about 0.45 to about 0.5, or from about 0.5 to about 0.55 mole fraction of the third monomer of formula (III). In certain embodiments, wherein the acrylated chitosan comprises from about 0.3 to about 0.6 mole fraction of the third monomer of formula (III). In certain embodiments, wherein the acrylated chitosan comprises from about 0.3 to about 0.45, about 0.4 to about 0.45 mole fraction, or about 0.4 to about 0.55 of the third monomer of formula (III).

In certain embodiments, the acrylated chitosan further comprises less than about 0.1 mole fraction of a fourth monomer of formula (IV)

In certain embodiments, the acrylated chitosan further comprises less than about 0.03 mole fraction of the fourth monomer of formula (IV). In certain embodiments, the acrylated chitosan further comprises from about 0.01 to about 0.03, from about 0.015 to about 0.03, from about 0.02 to about 0.03, from about 0.025 to about 0.03, from about 0.01 to about 0.025, from about 0.01 to about 0.02, from about 0.01 to about 0.015, from about 0.015 to about 0.025, from about 0.015 to about 0.02, or from about 0.02 to about 0.025 mole fraction of the fourth monomer of formula (IV). In certain embodiments, the acrylated chitosan further comprises from about 0.01 to about 0.03 mole fraction of the fourth monomer of formula (IV).

In certain embodiments, the acrylated chitosan has a Mw of from about 25 kDa to about 400 kDa, from about 25 kDa to about 300 kDa, from about 25 kDa to about 200 kDa, from about 50 kDa to about 400 kDa, from about 50 kDa to about 300 kDa, from about 50 kDa to about 200 kDa, from about 115 kDa to about 200 kDa, from about 115 kDa to about 175 kDa, from about 115 kDa to about 165 kDa, from about 115 kDa to about 155 kDa, from about 115 kDa to about 145 kDa, from about 115 kDa to about 135 kDa, from about 115 kDa to about 125 kDa, from about 125 kDa to about 200 kDa, from about 125 kDa to about 175 kDa, from about 125 kDa to about 165 kDa, from about 125 kDa to about 155 kDa, from about 125 kDa to about 145 kDa, from about 125 kDa to about 135 kDa, from about 135 kDa to about 200 kDa, from about 135 kDa to about 175 kDa, from about 135 kDa to about 165 kDa, from about 135 kDa to about 155 kDa, from about 135 kDa to about 145 kDa, from about 145 kDa to about 200 kDa, from about 145 kDa to about 175 kDa, from about 145 kDa to about 165 kDa, from about 145 kDa to about 155 kDa, from about 155 kDa to about 200 kDa, from about 155 kDa to about 175 kDa, from about 155 kDa to about 165 kDa, from about 165 kDa to about 200 kDa, from about 165 kDa to about 175 kDa, or from about 175 kDa to about 200 kDa.

In certain embodiments, the acrylated chitosan has a Mw of from about 25 kDa to about 400 kDa. In certain embodiments, the acrylated chitosan has a Mw of from about 115 kDa to about 200 kDa. In certain embodiments, the acrylated chitosan has a Mw of from about 115 kDa to about 165 kDa, from about 125 kDa to about 155 kDa, or from about 135 kDa to about 175 kDa.

In certain embodiments, the acrylated chitosan has a Mn of from about 14 kDa to about 200 kDa, from about 14 kDa to about 150 kDa, from about 25 kDa to about 200 kDa, from about 14 kDa to about 150 kDa, from about 55 kDa to about 140 kDa, from about 55 kDa to about 120 kDa, from about 55 kDa to about 100 kDa, from about 55 kDa to about 90 kDa, from about 55 kDa to about 80 kDa, from about 55 kDa to about 75 kDa, from about 55 kDa to about 70 kDa, from about 55 kDa to about 65 kDa, from about 55 kDa to about 60 kDa, from about 60 kDa to about 140 kDa, from about 60 kDa to about 120 kDa, from about 60 kDa to about 100 kDa, from about 60 kDa to about 90 kDa, from about 60 kDa to about 80 kDa, from about 60 kDa to about 75 kDa, from about 60 kDa to about 70 kDa, from about 60 kDa to about 65 kDa, from about 65 kDa to about 140 kDa, from about 65 kDa to about 120 kDa, from about 65 kDa to about 100 kDa, from about 65 kDa to about 90 kDa, from about 65 kDa to about 80 kDa, from about 65 kDa to about 75 kDa, from about 65 kDa to about 70 kDa, from about 70 kDa to about 140 kDa, from about 70 kDa to about 120 kDa, from about 70 kDa to about 100 kDa, from about 70 kDa to about 90 kDa, from about 70 kDa to about 80 kDa, from about 70 kDa to about 75 kDa, from about 75 kDa to about 140 kDa, from about 75 kDa to about 120 kDa, from about 75 kDa to about 100 kDa, from about 75 kDa to about 90 kDa, from about 75 kDa to about 80 kDa, from about 80 kDa to about 140 kDa, from about 80 kDa to about 120 kDa, from about 80 kDa to about 100 kDa, from about 80 kDa to about 90 kDa, from about 90 kDa to about 140 kDa, from about 90 kDa to about 120 kDa, from about 90 kDa to about 100 kDa, from about 100 kDa to about 140 kDa, from about 100 kDa to about 120 kDa, or from about 120 kDa to about 140 kDa.

In certain embodiments, the acrylated chitosan has a Mn of from about 14 kDa to about 200 kDa. In certain embodiments, the acrylated chitosan has a Mn of from about 55 kDa to about 140 kDa. In certain embodiments, the acrylated chitosan has a Mn of from about 55 kDa to about 75 kDa, from about 65 kDa to about 75 kDa, or from about 65 kDa to about 100 kDa.

In certain embodiments, the acrylated chitosan has a PDI of from about 1.5 (Mw/Mn) to about 3.5 (Mw/Mn), from about 1.7 (Mw/Mn) to about 3.5 (Mw/Mn), from about 2.1 (Mw/Mn) to about 3.5 (Mw/Mn), from about 2.4 (Mw/Mn) to about 3.5 (Mw/Mn), from about 2.7 (Mw/Mn) to about 3.5 (Mw/Mn), from about 3.0 (Mw/Mn) to about 3.5 (Mw/Mn), from about 3.3 (Mw/Mn) to about 3.5 (Mw/Mn), from about 1.5 (Mw/Mn) to about 3.3 (Mw/Mn), from about 1.5 (Mw/Mn) to about 3.0 (Mw/Mn), from about 1.5 (Mw/Mn) to about 2.7 (Mw/Mn), from about 1.5 (Mw/Mn) to about 2.4 (Mw/Mn), from about 1.5 (Mw/Mn) to about 2.1 (Mw/Mn), from about 1.5 (Mw/Mn) to about 1.8 (Mw/Mn), from about 1.7 (Mw/Mn) to about 3.3 (Mw/Mn), from about 1.7 (Mw/Mn) to about 3.0 (Mw/Mn), from about 1.7 (Mw/Mn) to about 2.7 (Mw/Mn), from about 1.7 (Mw/Mn) to about 2.4 (Mw/Mn), from about 1.7 (Mw/Mn) to about 2.1 (Mw/Mn), from about 1.9 (Mw/Mn) to about 3.3 (Mw/Mn), from about 1.9 (Mw/Mn) to about 3.0 (Mw/Mn), from about 1.9 (Mw/Mn) to about 2.7 (Mw/Mn), from about 1.9 (Mw/Mn) to about 2.4 (Mw/Mn), from about 1.9 (Mw/Mn) to about 2.1 (Mw/Mn), from about 2.1 (Mw/Mn) to about 3.3 (Mw/Mn), from about 2.1 (Mw/Mn) to about 3.0 (Mw/Mn), from about 2.1 (Mw/Mn) to about 2.7 (Mw/Mn), from about 2.1 (Mw/Mn) to about 2.4 (Mw/Mn), from about 2.3 (Mw/Mn) to about 3.3 (Mw/Mn), from about 2.3 (Mw/Mn) to about 3.0 (Mw/Mn), from about 2.3 (Mw/Mn) to about 2.7 (Mw/Mn), from about 2.3 (Mw/Mn) to about 2.4 (Mw/Mn), from about 2.5 (Mw/Mn) to about 3.3 (Mw/Mn), from about 2.5 (Mw/Mn) to about 3.0 (Mw/Mn), from about 2.5 (Mw/Mn) to about 2.7 (Mw/Mn), from about 2.7 (Mw/Mn) to about 3.3 (Mw/Mn), from about 2.7 (Mw/Mn) to about 3.0 (Mw/Mn), from about 2.9 (Mw/Mn) to about 3.3 (Mw/Mn), from about 2.9 (Mw/Mn) to about 3.0 (Mw/Mn), or from about 3.1 (Mw/Mn) to about 3.3 (Mw/Mn).

In certain embodiments, the acrylated chitosan has a PDI of from about 1.5 (Mw/Mn) to about 3.5 (Mw/Mn). In certain embodiments, the acrylated chitosan has a PDI of from about 1.5 (Mw/Mn) to about 2.4 (Mw/Mn), from about 1.7 (Mw/Mn) to about 2.1 (Mw/Mn), or from about 2.1 (Mw/Mn) to about 3.0 (Mw/Mn).

In certain embodiments, the acrylated chitosan has a Mz of from about 80 kDa to about 1,200 kDa, from about 80 kDa to about 600 kDa, from about 80 kDa to about 500 kDa, from about 80 kDa to about 370 kDa, from about 150 kDa to about 1,200 kDa, from about 150 kDa to about 600 kDa, from about 150 kDa to about 500 kDa, from about 150 kDa to about 370 kDa, from about 200 kDa to about 500 kDa, from about 200 kDa to about 370 kDa, from about 200 kDa to about 350 kDa, from about 200 kDa to about 320 kDa, from about 200 kDa to about 300 kDa, from about 200 kDa to about 270 kDa, from about 200 kDa to about 260 kDa, from about 200 kDa to about 250 kDa, from about 200 kDa to about 240 kDa, from about 200 kDa to about 230 kDa, from about 200 kDa to about 220 kDa, from about 200 kDa to about 210 kDa, from about 210 kDa to about 370 kDa, from about 210 kDa to about 350 kDa, from about 210 kDa to about 320 kDa, from about 210 kDa to about 300 kDa, from about 210 kDa to about 270 kDa, from about 210 kDa to about 260 kDa, from about 210 kDa to about 250 kDa, from about 210 kDa to about 240 kDa, from about 210 kDa to about 230 kDa, from about 210 kDa to about 220 kDa, from about 220 kDa to about 370 kDa, from about 220 kDa to about 350 kDa, from about 220 kDa to about 320 kDa, from about 220 kDa to about 300 kDa, from about 220 kDa to about 270 kDa, from about 220 kDa to about 260 kDa, from about 220 kDa to about 250 kDa, from about 220 kDa to about 240 kDa, from about 220 kDa to about 230 kDa, from about 230 kDa to about 370 kDa, from about 230 kDa to about 350 kDa, from about 230 kDa to about 320 kDa, from about 230 kDa to about 300 kDa, from about 230 kDa to about 270 kDa, from about 230 kDa to about 260 kDa, from about 230 kDa to about 250 kDa, from about 230 kDa to about 240 kDa, from about 240 kDa to about 370 kDa, from about 240 kDa to about 350 kDa, from about 240 kDa to about 320 kDa, from about 240 kDa to about 300 kDa, from about 240 kDa to about 270 kDa, from about 240 kDa to about 260 kDa, from about 240 kDa to about 250 kDa, from about 250 kDa to about 370 kDa, from about 250 kDa to about 350 kDa, from about 250 kDa to about 320 kDa, from about 250 kDa to about 300 kDa, from about 250 kDa to about 270 kDa, from about 250 kDa to about 260 kDa, from about 260 kDa to about 370 kDa, from about 260 kDa to about 350 kDa, from about 260 kDa to about 320 kDa, from about 260 kDa to about 300 kDa, from about 260 kDa to about 270 kDa, from about 270 kDa to about 370 kDa, from about 270 kDa to about 350 kDa, from about 270 kDa to about 320 kDa, from about 270 kDa to about 300 kDa, from about 300 kDa to about 370 kDa, from about 300 kDa to about 350 kDa, from about 300 kDa to about 320 kDa, from about 320 kDa to about 370 kDa, from about 320 kDa to about 350 kDa, or from about 350 kDa to about 370 kDa.

In certain embodiments, the acrylated chitosan has a Mz of from about 80 kDa to about 1,200 kDa. In certain embodiments, the acrylated chitosan has a Mz of from about 200 kDa to about 350 kDa. In certain embodiments, the acrylated chitosan has a Mz of from about 200 kDa to about 500 kDa. In certain embodiments, the acrylated chitosan has a Mz of from about 200 kDa to about 300 kDa, from about 210 kDa to about 370 kDa, or from about 250 kDa to about 370 kDa.

In certain embodiments, the acrylated chitosan has a PDI of from about 1.5 (Mz/Mw) to about 7.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 5.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 3.0 (Mz/Mw), from about 1.6 (Mz/Mw) to about 3.0 (Mz/Mw), from about 1.6 (Mz/Mw) to about 2.5 (Mz/Mw), from about 1.6 (Mz/Mw) to about 2.0 (Mz/Mw), from about 1.6 (Mz/Mw) to about 1.9 (Mz/Mw), from about 1.6 (Mz/Mw) to about 1.8 (Mz/Mw), from about 1.6 (Mz/Mw) to about 1.7 (Mz/Mw), from about 1.7 (Mz/Mw) to about 3.0 (Mz/Mw), from about 1.7 (Mz/Mw) to about 2.5 (Mz/Mw), from about 1.7 (Mz/Mw) to about 2.0 (Mz/Mw), from about 1.7 (Mz/Mw) to about 1.9 (Mz/Mw), from about 1.7 (Mz/Mw) to about 1.8 (Mz/Mw), from about 1.8 (Mz/Mw) to about 3.0 (Mz/Mw), from about 1.8 (Mz/Mw) to about 2.5 (Mz/Mw), from about 1.8 (Mz/Mw) to about 2.0 (Mz/Mw), from about 1.8 (Mz/Mw) to about 1.9 (Mz/Mw), from about 1.9 (Mz/Mw) to about 3.0 (Mz/Mw), from about 1.9 (Mz/Mw) to about 2.5 (Mz/Mw), from about 1.9 (Mz/Mw) to about 2.0 (Mz/Mw), from about 2.0 (Mz/Mw) to about 3.0 (Mz/Mw), from about 2.0 (Mz/Mw) to about 2.5 (Mz/Mw), or from about 2.5 (Mz/Mw) to about 3.0 (Mz/Mw).

In certain embodiments, the acrylated chitosan has a PDI of from about 1.5 (Mz/Mw) to about 7.0 (Mz/Mw). In certain embodiments, the acrylated chitosan has a PDI of from about 1.6 (Mz/Mw) to about 3.0 (Mz/Mw). In certain embodiments, the acrylated chitosan has a PDI of from about 1.5 (Mz/Mw) to about 2.0 (Mz/Mw), from about 1.6 (Mz/Mw) to about 2.5 (Mz/Mw), from about 1.9 (Mz/Mw) to about 3.0 (Mz/Mw).

In certain embodiments, the acrylated chitosan composition comprises about 1% (w/w), about 2% (w/w), about 3% (w/w), about 4% (w/w), about 5% (w/w), about 6% (w/w), about 7% (w/w), about 8% (w/w), about 9% (w/w), about 10% (w/w), about 11% (w/w), about 12% (w/w), about 13% (w/w), about 14% (w/w), about 15% (w/w), about 16% (w/w), about 17% (w/w), about 18% (w/w), about 19% (w/w), about 20% (w/w), about 21% (w/w), about 22% (w/w), about 23% (w/w), about 24% (w/w), or about 25% (w/w) of the acrylated chitosan.

In certain embodiments, the acrylated chitosan composition comprises from about 1% (w/w) to about 25% (w/w), from about 1% (w/w) to about 20% (w/w), from about 1% (w/w) to about 15% (w/w), from about 1% (w/w) to about 10% (w/w), from about 1% (w/w) to about 9% (w/w), from about 1% (w/w) to about 8% (w/w), from about 1% (w/w) to about 7% (w/w), from about 1% (w/w) to about 6% (w/w), from about 1% (w/w) to about 5% (w/w), from about 1% (w/w) to about 4% (w/w), from about 1% (w/w) to about 3% (w/w), from about 1% (w/w) to about 2% (w/w), from about 2% (w/w) to about 10% (w/w), from about 2% (w/w) to about 9% (w/w), from about 2% (w/w) to about 8% (w/w), from about 2% (w/w) to about 7% (w/w), from about 2% (w/w) to about 6% (w/w), from about 2% (w/w) to about 5% (w/w), from about 2% (w/w) to about 4% (w/w), from about 2% (w/w) to about 3% (w/w), from about 3% (w/w) to about 10% (w/w), from about 3% (w/w) to about 9% (w/w), from about 3% (w/w) to about 8% (w/w), from about 3% (w/w) to about 7% (w/w), from about 3% (w/w) to about 6% (w/w), from about 3% (w/w) to about 5% (w/w), from about 3% (w/w) to about 4% (w/w), from about 4% (w/w) to about 10% (w/w), from about 4% (w/w) to about 9% (w/w), from about 4% (w/w) to about 8% (w/w), from about 4% (w/w) to about 7% (w/w), from about 4% (w/w) to about 6% (w/w), from about 4% (w/w) to about 5% (w/w), from about 5% (w/w) to about 10% (w/w), from about 5% (w/w) to about 9% (w/w), from about 5% (w/w) to about 8% (w/w), from about 5% (w/w) to about 7% (w/w), from about 5% (w/w) to about 6% (w/w), from about 6% (w/w) to about 10% (w/w), from about 6% (w/w) to about 9% (w/w), from about 6% (w/w) to about 8% (w/w), from about 6% (w/w) to about 7% (w/w), from about 7% (w/w) to about 10% (w/w), from about 7% (w/w) to about 9% (w/w), from about 7% (w/w) to about 8% (w/w), from about 8% (w/w) to about 10% (w/w), from about 8% (w/w) to about 9% (w/w), or from about 9% (w/w) to about 10% (w/w) of the acrylated chitosan. In certain embodiments, the acrylated chitosan composition comprises from about 1% (w/w) to about 25% (w/w) of the acrylated chitosan. In certain embodiments, the acrylated chitosan composition comprises from about 1% (w/w) to about 10% (w/w) of the acrylated chitosan. In certain embodiments, the acrylated chitosan composition comprises from about 2% (w/w) to about 5% (w/w), from about 4% (w/w) to about 7% (w/w), or from about 6% (w/w) to about 9% (w/w) of the acrylated chitosan.

In certain embodiments, the acrylated chitosan composition has a viscosity of from about 10 cP to about 50,000 cP, from about 10 cP to about 35,000 cP, from about 10 cP to about 25,000 cP, from about 10 cP to about 20,000 cP, from about 10 cP to about 10,000 cP, from about 10 cP to about 8,000 cP, from about 10 cP to about 4,000 cP, from about 10 cP to about 1,000 cP, from about 10 cP to about 100 cP, from about 100 cP to about 25,000 cP, from about 100 cP to about 20,000 cP, from about 100 cP to about 10,000 cP, from about 100 cP to about 8,000 cP, from about 100 cP to about 4,000 cP, from about 100 cP to about 1,000 cP, from about 1,000 cP to about 25,000 cP, from about 1,000 cP to about 20,000 cP, from about 1,000 cP to about 10,000 cP, from about 1,000 cP to about 8,000 cP, from about 1,000 cP to about 4,000 cP, from about 4,000 cP to about 25,000 cP, from about 4,000 cP to about 20,000 cP, from about 4,000 cP to about 10,000 cP, from about 4,000 cP to about 8,000 cP, from about 8,000 cP to about 25,000 cP, from about 8,000 cP to about 20,000 cP, from about 8,000 cP to about 10,000 cP, or from about 10,000 cP to about 20,000 cP.

In certain embodiments, the acrylated chitosan composition has a viscosity of from about 10 cP to about 50,000 cP. In certain embodiments, the acrylated chitosan composition has a viscosity of from about 100 cP to about 25,000 cP. In certain embodiments, the acrylated chitosan composition has a viscosity of from about 1,000 cP to about 10,000 cP, about 8,000 cP to about 20,000 cP, or from about 10,000 cP to about 25,000 cP.

In certain embodiments, the acrylated chitosan composition has a pH of from about 5.5 to about 9.0, from about 6.0 to about 9.0, from about 6.5 to about 9.0, from about 7.0 to about 9.0, from about 7.5 to about 9.0, from about 8.0 to about 9.0, from about 8.5 to about 9.0, from about 8.0 to about 8.8, from about 8.0 to about 8.6, from about 8.0 to about 8.4, from about 8.0 to about 8.2, from about 8.2 to about 8.8, from about 8.2 to about 8.6, from about 8.2 to about 8.4, from about 8.4 to about 8.8, from about 8.4 to about 8.6, or from about 8.6 to about 8.8. In certain embodiments, the acrylated chitosan composition has a pH of from about 5.5 to about 9.0. In certain embodiments, the acrylated chitosan composition has a pH of from about 8.0 to about 8.4, from about 8.2 to about 8.8, or from about 8.2 to about 8.8.

In certain embodiments, the acrylated chitosan composition has a conductivity of from about 0.75 (mS/cm) to about 25.0 (mS/cm), from about 0.75 (mS/cm) to about 20.0 (mS/cm), from about 0.75 (mS/cm) to about 15.0 (mS/cm), from about 0.75 (mS/cm) to about 10.0 (mS/cm), from about 0.75 (mS/cm) to about 5.0 (mS/cm), from about 0.75 (mS/cm) to about 4.0 (mS/cm), from about 0.75 (mS/cm) to about 3.0 (mS/cm), from about 0.75 (mS/cm) to about 2.0 (mS/cm), from about 0.75 (mS/cm) to about 1.0 (mS/cm), from about 1.0 (mS/cm) to about 10.0 (mS/cm), from about 1.0 (mS/cm) to about 5.0 (mS/cm), from about 1.0 (mS/cm) to about 4.0 (mS/cm), from about 1.0 (mS/cm) to about 3.0 (mS/cm), from about 1.0 (mS/cm) to about 2.0 (mS/cm), from about 2.0 (mS/cm) to about 10.0 (mS/cm), from about 2.0 (mS/cm) to about 5.0 (mS/cm), from about 2.0 (mS/cm) to about 4.0 (mS/cm), from about 2.0 (mS/cm) to about 3.0 (mS/cm), from about 3.0 (mS/cm) to about 10.0 (mS/cm), from about 3.0 (mS/cm) to about 5.0 (mS/cm), from about 3.0 (mS/cm) to about 4.0 (mS/cm), from about 4.0 (mS/cm) to about 10.0 (mS/cm), from about 4.0 (mS/cm) to about 5.0 (mS/cm), or from about 5.0 (mS/cm) to about 10.0 (mS/cm).

In certain embodiments, the acrylated chitosan composition has a conductivity of from about 0.75 (mS/cm) to about 25.0 (mS/cm). In certain embodiments, the acrylated chitosan composition has a conductivity of from about 0.75 (mS/cm) to about 10 (mS/cm). In certain embodiments, the acrylated chitosan composition has a conductivity of from about 1.0 (mS/cm) to about 5.0 (mS/cm), from about 3.0 (mS/cm) to about 10.0 (mS/cm), or from about 5.0 (mS/cm) to about 10.0 (mS/cm).

In certain embodiments, the acrylated chitosan has two or more properties selected from a Mw of from about 25 kDa to about 400 kDa, a Mn of from about 14 kDa to about 200 kDa, a PDI of from about 1.5 to about 3.5 (Mw/Mn), a Mz of from about 80kDa to about 1,200 kDa, and a PDI of from about 1.5 to about 7.0 (Mz/Mw).

In certain embodiments, the acrylated chitosan composition comprises a plurality (e.g., 2, 3, 4, 5, 6, 7, or 8) or all of the following features: (i) a Mw of from about 115 kDa to about 200 kDa, (ii) a Mn of from about 55 kDa to about 140 kDa, (iii) a Mz of from about 200 kDa to about 500 kDa, (iv) a PDI (Mw/Mn) of from about 1.5 to about 3.5, (v) a PDI (Mz/Mw) of from about 1.6 to about 3.0, (vi) a mole fraction of the monomer of formula (I) of from about 0.011 to about 0.26, (vii) a mole fraction of the monomer of formula (II) of from about 0.35 to about 0.65, (viii) a mole fraction of the monomer of formula (III) of from about 0.32 to about 0.6, and (ix) a mole fraction of the monomer of formula (IV) of from about 0.009 to about 0.028.

In certain embodiments, the acrylated chitosan composition comprises a plurality (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12) or all of the following features: (i) a Mw of from about 115 kDa to about 200 kDa, (ii) a Mn of from about 55 kDa to about 140 kDa, (iii) a Mz of from about 200 kDa to about 500 kDa, (iv) a PDI (Mw/Mn) of from about 1.5 to about 3.5, (v) a PDI (Mz/Mw) of from about 1.6 to about 3.0, (vi) a mole fraction of the monomer of formula (I) of from about 0.011 to about 0.26, (vii) a mole fraction of the monomer of formula (II) of from about 0.35 to about 0.65, (viii) a mole fraction of the monomer of formula (III) of from about 0.32 to about 0.6, (ix) a mole fraction of the monomer of formula (IV) of from about 0.009 to about 0.028, (x) a concentration of the acrylated chitosan in an aqueous medium of from about 1% (w/w) to about 10% (w/w), (xi) a viscosity of from about 10 cP to about 20,300 cP, (xii) a pH of from about 5.5 to about 9.0, and (xiii) a conductivity of from about 0.75 mS/cm to about 10.0 mS/cm.

The acrylated chitosan described in this section II can be produced by the methodologies described in section III below.

III Methods of Making Acrylated Chitosan

In one aspect, the invention provides a method of preparing an acrylated chitosan composition useful in making a hemostatic hydrogel composition described herein. The method comprises the steps of:

-   -   (a) contacting a raw chitosan material with an aqueous organic         acid solution to form a chitosan intermediate;     -   (b) contacting the chitosan intermediate material with an         α,β-unsaturated carboxylic acid to form an acrylated chitosan         intermediate; and     -   (c) purifying the acrylated chitosan intermediate to produce an         acrylated chitosan composition of the present invention.

The step of contacting the raw chitosan material with the aqueous organic acid solution prior to the addition of the α,β-unsaturated carboxylic acid is important and has a significant effect on the structure and functionality of the resulting acrylated chitosan. In particular, the step of contacting the raw chitosan material with the aqueous organic acid solution permits the chitosan to dissolve and unwind or disentangle in solution prior to acrylation, and is believed to create a substantially homogeneous solution where the ammonium groups disposed throughout the chitosan are available to react with the α,β-unsaturated carboxylic acid to produce the acrylated chitosan. Under these conditions, it is believed that a large number of the ammonium groups are available for acrylation resulting in a random distribution of acrylate groups along the chitosan backbone to produce a substantially homogenous acrylated chitosan. In contrast, if raw chitosan is added to a stirred solution of acrylic acid in water (see Example 1 of U.S. Pat. No. 7,854,923), it is believed that the acrylation process occurs at a rate comparable to the rate of dissolution, and, as a result, as the chitosan dissolves, the soluble portions may be rapidly acrylated forming more blocky segments of acrylated groups along the chitosan backbone. Furthermore, using such an approach it is believed that lower molecular weight chains of chitosan may become more acrylated as they dissolve more quickly than higher molecular weight components. Collectively, it is believed that this results in substantially non-homogeneous acrylation with blocks of acrylate being distributed along the chitosan backbone.

The step of contacting the raw chitosan material with the organic acid in step (a) prior to acrylation creates a number of significant changes to the resulting chitosan, including, for example, (i) producing a more homogeneous chitosan solution, which when treated with the α,β-unsaturated carboxylic acid produces a more randomly acrylated chitosan than would otherwise be achievable without the step, (ii) reducing the z-average molecular weight (Mz) of the acrylated chitosan relative to the starting raw chitosan material, and (iii) reducing the amount of undesirable diacrylated monomer present in the resulting acrylated chitosan (see, for example, formula IV herein). The diacrylated chitosan (e.g., formula IV herein) is generally less desirable because it facilitates intermolecular ionic crosslinking that decreases solubility and increases the viscosity of the acrylated chitosan solutions. As a result, acrylated chitosan produced by the method described herein is particularly advantageous when combined with the oxidized dextran described herein to produce hemostatic hydrogel.

In certain embodiments, the acrylated chitosan produced in step (c) is the acrylated chitosan composition described herein.

In certain embodiments, during step (a), the raw chitosan material is contacted with the aqueous organic acid solution at a pressure of about 0.5 atmospheres, about 1.0 atmosphere, about 1.5 atmospheres, about 2 atmospheres, about 2.5 atmospheres, about 3.0 atmospheres, about 3.5 atmospheres, about 4.0 atmospheres, about 4.5 atmospheres, or about 5.0 atmospheres. In certain embodiments, during step (a), the raw chitosan material is contacted with the aqueous organic acid solution at a pressure of about 2 atmospheres.

In certain embodiments, during step (a), the raw chitosan material is contacted with the aqueous organic acid solution at a temperature of about 80° C., about 85° C., about 90° C., about 95° C., about 100° C., about 115° C., or about 120° C. In certain embodiments, during step (a), the raw chitosan material is contacted with the aqueous organic acid solution at a temperature of from about 80° C. to about 120° C., from about 90° C. to about 120° C., from about 100° C. to about 120° C., from about 110° C. to about 120° C., from about 80° C. to about 110° C., from about 80° C. to about 100° C., from about 80° C. to about 90° C., from about 90° C. to about 110° C., from about 90° C. to about 100° C., or from about 100° C. to about 110° C. In certain embodiments, during step (a), the raw chitosan material is contacted with the aqueous organic acid solution at a temperature of from about 80° C. to about 120° C.

In certain embodiments, during step (a), the aqueous organic acid solution is a 1% (v/v) aqueous organic acid solution, a 2% (v/v) aqueous organic acid solution, a 3% (v/v) aqueous organic acid solution, a 4% (v/v) aqueous organic acid solution, a 5% (v/v) aqueous organic acid solution, a 6% (v/v) aqueous organic acid solution, a 7% (v/v) aqueous organic acid solution, a 8% (v/v) aqueous organic acid solution, a 9% (v/v) aqueous organic acid solution, or a 10% (v/v) aqueous organic acid solution. In certain embodiments, during step (a), the aqueous organic acid solution is a 1% (v/v) aqueous organic acid solution.

In certain embodiments, during step (a), the aqueous organic acid solution is a 1% (w/v) aqueous organic acid solution, a 2% (w/v) aqueous organic acid solution, a 3% (w/v) aqueous organic acid solution, a 4% (w/v) aqueous organic acid solution, a 5% (w/v) aqueous organic acid solution, a 6% (w/v) aqueous organic acid solution, a 7% (w/v) aqueous organic acid solution, a 8% (w/v) aqueous organic acid solution, a 9% (w/v) aqueous organic acid solution, or a 10% (w/v) aqueous organic acid solution. In certain embodiments, during step (a), the aqueous organic acid solution is a 1% (w/v) aqueous organic acid solution.

Examples of organic acids include, but are not limited to, acetic acid, citric acid, formic acid, lactic acid, malic acid, oxalic acid, and uric acid. In certain embodiments, the organic acid is acetic acid.

In certain embodiments, during step (a), the raw chitosan material has a weight-average molecular weight (Mw) of from about 40 kDa to about 1,000 kDa, from about 50 kDa to about 750 kDa, from about 50 kDa to about 500 kDa, from about 50 kDa to about 400 kDa, from about 50 kDa to about 300 kDa, from about 50 kDa to about 200 kDa, from about 100 kDa to about 750 kDa, from about 100 kDa to about 500 kDa, from about 100 kDa to about 450 kDa, from about 100 kDa to about 400 kDa, from about 100 kDa to about 350 kDa, from about 100 kDa to about 300 kDa, from about 100 kDa to about 250 kDa, from about 100 kDa to about 200 kDa, from about 100 kDa to about 150 kDa, from about 150 kDa to about 500 kDa, from about 150 kDa to about 450 kDa, from about 150 kDa to about 400 kDa, from about 150 kDa to about 350 kDa, from about 150 kDa to about 300 kDa, from about 150 kDa to about 250 kDa, from about 150 kDa to about 200 kDa, from about 200 kDa to about 500 kDa, from about 200 kDa to about 450 kDa, from about 200 kDa to about 400 kDa, from about 200 kDa to about 350 kDa, from about 200 kDa to about 300 kDa, from about 200 kDa to about 250 kDa, from about 250 kDa to about 500 kDa, from about 250 kDa to about 450 kDa, from about 250 kDa to about 400 kDa, from about 250 kDa to about 350 kDa, from about 250 kDa to about 300 kDa, from about 300 kDa to about 500 kDa, from about 300 kDa to about 450 kDa, from about 300 kDa to about 400 kDa, from about 300 kDa to about 350 kDa, from about 350 kDa to about 500 kDa, from about 350 kDa to about 450 kDa, from about 350 kDa to about 400 kDa, from about 400 kDa to about 500 kDa, from about 400 kDa to about 450 kDa, or from about 450 kDa to about 500 kDa. In certain embodiments, during step (a), the raw chitosan material has a Mw of from about 40 kDa to about 1,000 kDa. In certain embodiments, during step (a), the raw chitosan material has a Mw of from about 100 kDa to about 500 kDa. In certain embodiments, during step (a), the raw chitosan material has a Mw of from about 100 kDa to about 250 kDa, from about 150 kDa to about 350 kDa, from about 200 kDa to about 350 kDa, from about 200 kDa to about 300 kDa, from about 250 kDa to about 300 kDa, or from about 300 kDa to about 450 kDa. In certain embodiments, during step (a), the raw chitosan material has a Mw of from about 150 kDa to about 350 kDa. In certain embodiments, during step (a), the raw chitosan material has a Mw of from about 200 kDa to about 300 kDa. In certain embodiments, during step (a), the raw chitosan material has a Mw of from about 250 kDa to about 300 kDa. In certain embodiments, during step (a), the raw chitosan material has a Mw of from about 50 kDa to about 200 kDa.

In certain embodiments, during step (a), the raw chitosan material has a Mw of less than 100 kDa, less than 200 kDa, less than 300 kDa, less than 400 kDa, less than 500 kDa, less than 600 kDa, less than 700 kDa, less than 800 kDa, less than 900 kDa, or less than 1000 kDa. In certain embodiments, during step (a), the raw chitosan material has a Mw of less than 200 kDa.

In certain embodiments, during step (a), the raw chitosan material has a number-average molecular weight (Mn) of greater than 10 kDa, greater than 15 kDa, greater than 20 kDa, greater than 25 kDa, greater than 30 kDa, greater than 35 kDa, greater than 40 kDa, greater than 45 kDa, greater than 50 kDa, greater than 55 kDa, greater than 60 kDa, greater than 65 kDa, greater than 70 kDa, greater than 75 kDa, greater than 80 kDa, greater than 85 kDa, greater than 90 kDa, greater than 95 kDa, greater than 100 kDa, greater than 105 kDa, greater than 110 kDa, greater than 115 kDa, greater than 120 kDa. In certain embodiments, during step (a), the raw chitosan material has a number-average molecular weight (Mn) of greater than 20 kDa. In certain embodiments, during step (a), the raw chitosan material has a number-average molecular weight (Mn) of greater than 60 kDa. In certain embodiments, during step (a), the raw chitosan material has a number-average molecular weight (Mn) of greater than 90 kDa.

In certain embodiments, during step (a), the raw chitosan material has a number-average molecular weight (Mn) in the range of from about 20 kDa to about 650 kDa, from about 20 kDa to about 400 kDa, from about 20 kDa to about 300 kDa, from about 20 kDa to about 200 kDa, from about 40 kDa to about 400 kDa, from about 40 kDa to about 300 kDa, from about 40 kDa to about 200 kDa, from about 40 kDa to about 100 kDa, from about 100 kDa to about 300 kDa, from about 100 kDa to about 200 kDa, or from about 200 kDa to about 300 kDa. In certain embodiments, during step (a), the raw chitosan material has a number-average molecular weight (Mn) in the range of from about 20 kDa to about 650 kDa. In certain embodiments, during step (a), the raw chitosan material has a number-average molecular weight (Mn) in the range of from about 40 kDa to about 300 kDa.

In certain embodiments, during step (a), the raw chitosan material has a polydispersity index (PDI) of from about 1.5 (Mw/Mn) to about 5.0 (Mw/Mn), from about 1.6 (Mw/Mn) to about 4.5 (Mw/Mn), from about 1.6 (Mw/Mn) to about 4.0 (Mw/Mn), from about 1.7 (Mw/Mn) to about 4.0 (Mw/Mn), from about 1.7 (Mw/Mn) to about 3.5 (Mw/Mn), from about 1.7 (Mw/Mn) to about 3.0 (Mw/Mn), from about 1.7 (Mw/Mn) to about 2.5 (Mw/Mn), from about 1.7 (Mw/Mn) to about 2.0 (Mw/Mn), from about 1.8 (Mw/Mn) to about 4.0 (Mw/Mn), from about 1.8 (Mw/Mn) to about 3.5 (Mw/Mn), from about 1.8 (Mw/Mn) to about 3.0 (Mw/Mn), from about 1.8 (Mw/Mn) to about 2.5 (Mw/Mn), from about 1.8 (Mw/Mn) to about 2.0 (Mw/Mn), from about 1.9 (Mw/Mn) to about 4.0 (Mw/Mn), from about 1.9 (Mw/Mn) to about 3.5 (Mw/Mn), from about 1.9 (Mw/Mn) to about 3.0 (Mw/Mn), from about 1.9 (Mw/Mn) to about 2.5 (Mw/Mn), from about 1.9 (Mw/Mn) to about 2.0 (Mw/Mn), from about 2.0 (Mw/Mn) to about 4.0 (Mw/Mn), from about 2.0 (Mw/Mn) to about 3.5 (Mw/Mn), from about 2.0 (Mw/Mn) to about 3.0 (Mw/Mn), from about 2.0 (Mw/Mn) to about 2.5 (Mw/Mn), from about 2.5 (Mw/Mn) to about 4.0 (Mw/Mn), from about 2.5 (Mw/Mn) to about 3.0 (Mw/Mn), or from about 3.0 (Mw/Mn) to about 4.0 (Mw/Mn). In certain embodiments, during step (a), the raw chitosan material has a polydispersity index of from about 1.5 (Mw/Mn) to about 5.0 (Mw/Mn). In certain embodiments, during step (a), the raw chitosan material has a polydispersity index of from about 1.7 (Mw/Mn) to about 4.0 (Mw/Mn). In certain embodiments, during step (a), the raw chitosan material has a polydispersity index of from about 1.6 (Mw/Mn) to about 3.0 (Mw/Mn), about 1.8 (Mw/Mn) to about 3.5 (Mw/Mn), from about 2.0 (Mw/Mn) to about 4.0 (Mw/Mn), or from about 2.5 (Mw/Mn) to about 3.0 (Mw/Mn). In certain embodiments, during step (a), the raw chitosan material has a polydispersity index of from about 1.8 (Mw/Mn) to about 3.5 (Mw/Mn). In certain embodiments, during step (a), the raw chitosan material has a polydispersity index of from about 2.5 (Mw/Mn) to about 3.0 (Mw/Mn).

In certain embodiments, during step (a), the raw chitosan material has a z-average molecular weight (Mz) of from about 100 kDa to about 2000 kDa, from about 100 kDa to about 1500 kDa, from about 100 kDa to about 1000 kDa, from about 200 kDa to about 2000 kDa, from about 100 kDa to about 15000 kDa, from about 100 kDa to about 1000 kDa, from about 250 kDa to about 750 kDa, from about 250 kDa to about 600 kDa, from about 250 kDa to about 550 kDa, from about 250 kDa to about 500 kDa, from about 250 kDa to about 400 kDa, from about 250 kDa to about 300 kDa, from about 300 kDa to about 750 kDa, from about 300 kDa to about 600 kDa, from about 300 kDa to about 550 kDa, from about 300 kDa to about 500 kDa, from about 300 kDa to about 400 kDa, from about 300 kDa to about 350 kDa, from about 350 kDa to about 750 kDa, from about 350 kDa to about 600 kDa, from about 350 kDa to about 550 kDa, from about 350 kDa to about 500 kDa, from about 350 kDa to about 400 kDa, from about 400 kDa to about 750 kDa, from about 400 kDa to about 600 kDa, from about 400 kDa to about 550 kDa, from about 400 kDa to about 500 kDa, from about 500 kDa to about 750 kDa, from about 500 kDa to about 600 kDa, from about 500 kDa to about 550 kDa, from about 550 kDa to about 750 kDa, from about 550 kDa to about 600 kDa, or from about 600 kDa to about 750 kDa. In certain embodiments, during step (a), the raw chitosan material has a Mz of from about 100 kDa to about 2000 kDa. In certain embodiments, during step (a), the raw chitosan material has a Mz of from about 250 kDa to about 750 kDa. In certain embodiments, during step (a), the raw chitosan material has a Mz of from about 250 kDa to about 500 kDa, from about 250 kDa to about 600 kDa, from about 350 kDa to about 600 kDa, from about 400 kDa to about 750 kDa, or from about 500 kDa to about 550 kDa.

In certain embodiments, during step (a), the raw chitosan material has a polydispersity index (PDI) of from about 1.5 (Mz/Mw) to about 4.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 3.75 (Mz/Mw), from about 1.5 (Mz/Mw) to about 3.5 (Mz/Mw), from about 1.5 (Mz/Mw) to about 3.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 2.5 (Mz/Mw), from about 1.5 (Mz/Mw) to about 2.0 (Mz/Mw), from about 2.0 (Mz/Mw) to about 3.75 (Mz/Mw), from about 2.0 (Mz/Mw) to about 3.5 (Mz/Mw), from about 2.0 (Mz/Mw) to about 3.0 (Mz/Mw), from about 2.0 (Mz/Mw) to about 2.5 (Mz/Mw), from about 2.5 (Mz/Mw) to about 3.75 (Mz/Mw), from about 2.5 (Mz/Mw) to about 3.5 (Mz/Mw), from about 2.5 (Mz/Mw) to about 3.0 (Mz/Mw), from about 3.0 (Mz/Mw) to about 3.75 (Mz/Mw) or from about 3.0 (Mz/Mw) to about 3.5 (Mz/Mw). In certain embodiments, during step (a), the raw chitosan material has a polydispersity index (PDI) of from about 1.5 (Mz/Mw) to about 4.0 (Mz/Mw). In certain embodiments, during step (a), the raw chitosan material has a polydispersity index (PDI) of from about 1.5 (Mz/Mw) to about 3.5 (Mz/Mw). In certain embodiments, during step (a), the raw chitosan material has a polydispersity index (PDI) of from about 1.5 (Mz/Mw) to about 2.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 2.5 (Mz/Mw), from about 1.5 (Mz/Mw) to about 3.0 (Mz/Mw), or from about 2.5 (Mz/Mw) to about 3.75 (Mz/Mw). In certain embodiments, during step (a), the raw chitosan material has a polydispersity index (PDI) of from about 1.5 (Mz/Mw) to about 3.0 (Mz/Mw). In certain embodiments, during step (a), the raw chitosan material has a polydispersity index (PDI) of from about 1.5 (Mz/Mw) to about 2.5 (Mz/Mw).

In certain embodiments, during step (a), the PDI (Mw/Mn) of the chitosan intermediate is from about 10% to about 60%, from about 10% to about 50%, from about 10% to about 40%, from about 15% to about 40%, from about 20% to about 40%, from about 30% to about 40%, from about 15% to about 30%, from about 15% to about 20%, or from about 20% to about 30% less than the PDI (Mw/Mn) of the raw chitosan material. In certain embodiments, during step (a), the PDI (Mw/Mn) of the chitosan intermediate is from about 10% to about 60% less than the PDI (Mw/Mn) of the raw chitosan material. In certain embodiments, during step (a), the PDI (Mw/Mn) of the chitosan intermediate is from about 15% to about 40% less than the PDI (Mw/Mn) of the raw chitosan material.

In certain embodiments, during step (a), the raw chitosan material has a degree of deacetylation of from about 65% to about 100%, from about 70% to about 100%, from about 75% to about 100%, from about 80% to about 100%, from about 85% to about 100%, from about 90% to about 100%, from about 95% to about 100%, about 65% to about 99%, from about 70% to about 99%, from about 72.5% to about 99%, from about 75% to about 99%, from about 77.5% to about 99%, from about 80.0% to about 99%, from about 85.0% to about 99%, about 65% to about 98%, from about 70% to about 98%, from about 72.5% to about 98%, from about 75% to about 98%, from about 77.5% to about 98%, from about 80.0% to about 98%, from about 85.0% to about 98%, about 65% to about 97%, from about 70% to about 97%, from about 72.5% to about 97%, from about 75% to about 97%, from about 77.5% to about 97%, from about 80.0% to about 97%, from about 85.0% to about 97%, about 65% to about 95%, from about 70% to about 95%, from about 72.5% to about 95%, from about 75% to about 95%, from about 77.5% to about 95%, from about 80.0% to about 95%, or from about 85.0% to about 95%. In certain embodiments, during step (a), the raw chitosan material has a degree of deacetylation of from about 65% to about 100%. In certain embodiments, during step (a), the raw chitosan material has a degree of deacetylation of from about 70% to about 98%. In certain embodiments, during step (a), the raw chitosan material has a degree of deacetylation of from about 65% to about 97%, from about 70% to about 98%, from about 75% to about 98%, from about 80% to about 99%, or from about 85.0% to about 95%. In certain embodiments, during step (a), the raw chitosan material has a degree of deacetylation of from about 75% to about 98%. In certain embodiments, during step (a), the raw chitosan material has a degree of deacetylation of from about 85% to about 95%.

In certain embodiments, the raw chitosan has two or more of the following features, a Mw of from about 100 kDa to about 500 kDa, a number-average molecular weight (Mn) in the range of from about 40 kDa to about 300 kDa, a PDI of from about 1.7 to about 4.0 (Mw/Mn), a z average molecular weight (Mz) of from about 250 kDa to about 750 kDa, a PDI from about 1.5 to about 4.0 (Mz/Mw), and a degree of deacetylation of from about 65% to about 100%.

In certain embodiments, during step (b), the chitosan intermediate is contacted with the α,β-unsaturated carboxylic acid at a temperature of about 50° C., about 60° C., about 70° C., about 80° C., about 90° C., about 100° C., about 110° C., or about 120° C. In certain embodiments, during step (b), the first chitosan intermediate is contacted with the α,β-unsaturated carboxylic acid at a temperature of from about 50° C. to about 120° C., from about 60° C. to about 120° C., from about 70° C. to about 120° C., from about 80° C. to about 120° C., from about 90° C. to about 120° C., from about 100° C. to about 120° C., from about 110° C. to about 120° C., from about 50° C. to about 110° C., from about 50° C. to about 100° C., from about 50° C. to about 90° C., from about 50° C. to about 80° C., from about 50° C. to about 70° C., from about 50° C. to about 60° C., from about 60° C. to about 110° C., from about 60° C. to about 100° C., from about 60° C. to about 90° C., from about 60° C. to about 80° C., from about 60° C. to about 70° C., from about 70° C. to about 110° C., from about 70° C. to about 100° C., from about 70° C. to about 90° C., from about 70° C. to about 80° C., from about 80° C. to about 110° C., from about 80° C. to about 100° C., from about 80° C. to about 90° C., from about 90° C. to about 110° C., from about 90° C. to about 100° C., or from about 100° C. to about 110° C. In certain embodiments, during step (b), the first chitosan intermediate is contacted with the α,β-unsaturated carboxylic acid at a temperature of from about 50° C. to about 100° C.

In certain embodiments, the α,β-unsaturated carboxylic acid is selected from the group consisting of acrylic acid, butenoic acid, methacrylic acid, and combinations thereof. In some embodiments, the α,β-unsaturated carboxylic acid is acrylic acid. In some embodiments, the α,β-unsaturated carboxylic acid is butenoic acid. In some embodiments, the α,β-unsaturated carboxylic acid is methacrylic acid.

In certain embodiments, the acrylated chitosan intermediate formed in step (b) has a degree of substitution (DS) value of from about 25% to about 65%.

In certain embodiments, during step (c), the acrylated chitosan intermediate is purified using a method selected from the group consisting of dialysis, gel filtration chromatography, stirred cell filtration, tangential flow filtration, and any combination thereof.

In certain embodiments, the yield of acrylated chitosan obtained following step (c) is from about 80% to about 100%, from about 85% to about 100%, from about 90% to about 100%, from about 95% to about 100%, from about 80% to about 95%, from about 80% to about 90%, from about 80% to about 85%, from about 85% to about 95%, from about 85% to about 90%, or from about 90% to about 95%. In certain embodiments, the yield of acrylated chitosan obtained following step (c) is from about 80% to about 97%.

In certain embodiments, the method further comprises the step of precipitating and/or lyophilizing the acrylated chitosan composition to provide a solid.

In certain embodiments, the method further comprises the step of dissolving the solid into an aqueous medium to form a solution comprising an amount of the acrylated chitosan composition of, for example, about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, about 10%, about 11%, about 12%, about 13%, about 14%, about 15%, about 16%, about 17%, about 18%, about 19%, about 20%, about 21%, about 22%, about 23%, about 24%, or about 25% by weight of the total weight of the solution.

In certain embodiments, the acrylated chitosan composition comprises from about 1% to about 25%, from about 1% to about 20%, from about 1% to about 15%, from about 1% to about 10%, from about 1% to about 9%, from about 1% to about 8%, from about 1% to about 7%, from about 1% to about 6%, from about 1% to about 5%, from about 1% to about 4%, from about 1% to about 3%, from about 1% to about 2%, from about 2% to about 10%, from about 2% to about 9%, from about 2% to about 8%, from about 2% to about 7%, from about 2% to about 6%, from about 2% to about 5%, from about 2% to about 4%, from about 2% to about 3%, from about 3% to about 10%, from about 3% to about 9%, from about 3% to about 8%, from about 3% to about 7%, from about 3% to about 6%, from about 3% to about 5%, from about 3% to about 4%, from about 4% to about 10%, from about 4% to about 9%, from about 4% to about 8%, from about 4% to about 7%, from about 4% to about 6%, from about 4% to about 5%, from about 5% to about 10%, from about 5% to about 9%, from about 5% to about 8%, from about 5% to about 7%, from about 5% to about 6%, from about 6% to about 10%, from about 6% to about 9%, from about 6% to about 8%, from about 6% to about 7%, from about 7% to about 10%, from about 7% to about 9%, from about 7% to about 8%, from about 8% to about 10%, from about 8% to about 9%, or from about 9% to about 10%, of the acrylated chitosan by weight of the total weight of the solution.

In certain embodiments, the acrylated chitosan composition comprises from about 1% to about 25% of the acrylated chitosan by weight of the total weight of the solution. In certain embodiments, the acrylated chitosan composition comprises from about 1% to about 10% of the acrylated chitosan by weight of the total weight of the solution. In certain embodiments, the acrylated chitosan composition comprises from about 2% to about 5%, from about 4% to about 7%, or from about 5% to about 9% of the acrylated chitosan by weight of the total weight of the solution.

In another aspect, provided herein is a method of preparing an acrylated chitosan composition comprising:

-   -   (a) contacting a raw chitosan material with an acetic acid         solution to form a chitosan intermediate, wherein the raw         chitosan material has a PDI of from about 1.5 (Mw/Mn) to about         5.0 (Mw/Mn);     -   (b) contacting the intermediate chitosan with acrylic acid to         form an acrylated chitosan intermediate having a degree of         substitution (DS) value of from about 25% to about 65%; and     -   (c) purifying the acrylated chitosan intermediate to produce an         acrylated chitosan composition of the present invention.

In certain embodiments, the acrylated chitosan produced in step (c) is the acrylated chitosan composition described herein.

In certain embodiments, the yield of acrylated chitosan obtained following step (c) is from about 80% to about 97%.

In certain embodiments, the method further comprising the step of precipitating the acrylated chitosan composition produced in step (c) to provide a solid. In certain embodiments, the method further comprising the step of lyophilizing the acrylated chitosan composition to provide a solid.

In certain embodiments, the method further comprising the step of dissolving the solid into an aqueous medium to form a solution comprising from about 1% to about 10% acrylated chitosan composition (w/w) of the total weight of the solution.

In another aspect, provided herein is an acrylated chitosan composition described herein produced by the methods described herein.

IV Oxidized Dextran Compositions

One aspect of the invention provides oxidized dextran compositions. In certain embodiments, the oxidized dextran compositions comprise an oxidized dextran comprising:

-   -   (i) less than about 0.8 mole fraction of a first monomer of         formula (V)

-   -    and     -   (ii) about 0.1 to about 1.0 mole fraction of a second monomer,         wherein the second monomer is selected from a monomer of formula         (VI), a monomer of formula (VII) and a combination of         formula (VI) and formula (VII)

In certain embodiments, the oxidized dextran comprises from about 0.5 to about 0.7, from about 0.52 to about 0.7, from about 0.54 to about 0.7, from about 0.56 to about 0.7, from about 0.58 to about 0.7, from about 0.6 to about 0.7, from about 0.62 to about 0.7, from about 0.64 to about 0.7, from about 0.66 to about 0.7, from about 0.68 to about 0.7, from about 0.5 to about 0.68, from about 0.5 to about 0.66, from about 0.5 to about 0.64, from about 0.5 to about 0.62, from about 0.5 to about 0.6, from about 0.5 to about 0.58, from about 0.5 to about 0.56, from about 0.5 to about 0.54, from about 0.5 to about 0.52, from about 0.52 to about 0.68, from about 0.52 to about 0.66, from about 0.52 to about 0.64, from about 0.52 to about 0.62, from about 0.52 to about 0.6, from about 0.52 to about 0.58, from about 0.52 to about 0.56, from about 0.52 to about 0.54, from about 0.54 to about 0.68, from about 0.54 to about 0.66, from about 0.54 to about 0.64, from about 0.54 to about 0.62, from about 0.54 to about 0.6, from about 0.54 to about 0.58, from about 0.54 to about 0.56, from about 0.56 to about 0.68, from about 0.56 to about 0.66, from about 0.56 to about 0.64, from about 0.56 to about 0.62, from about 0.56 to about 0.6, from about 0.56 to about 0.58, from about 0.58 to about 0.68, from about 0.58 to about 0.66, from about 0.58 to about 0.64, from about 0.58 to about 0.62, from about 0.58 to about 0.6, from about 0.6 to about 0.68, from about 0.6 to about 0.66, from about 0.6 to about 0.64, from about 0.6 to about 0.62, from about 0.62 to about 0.68, from about 0.62 to about 0.66, from about 0.62 to about 0.64, from about 0.64 to about 0.68, from about 0.64 to about 0.66, or from about 0.66 to about 0.68 mole fraction of the first monomer of formula (V). In certain embodiments, the oxidized dextran comprises from about 0.4 to about 0.7 mole fraction of the first monomer of formula (V). In certain embodiments, the oxidized dextran comprises from about 0.52 to about 0.6, about 0.56 to about 0.62, or about 0.6 to about 0.66 mole fraction of the first monomer of formula (V).

In certain embodiments, the oxidized dextran comprises from about 0.15 to about 0.35, from about 0.2 to about 0.35, from about 0.25 to about 0.35, from about 0.3 to about 0.35, from about 0.15 to about 0.3, from about 0.15 to about 0.25, from about 0.15 to about 0.2, from about 0.2 to about 0.3, from about 0.2 to about 0.25, or from about 0.25 to about 0.3 mole fraction of the second monomer. In certain embodiments, the oxidized dextran comprises from about 0.15 to about 0.35 mole fraction of the second monomer. In certain embodiments, the oxidized dextran comprises from about 0.15 to about 0.25, about 0.2 to about 0.3, or about 0.25 to about 0.35 mole fraction of the second monomer.

In certain embodiments, wherein the oxidized dextran further comprises less than about 0.65 mole fraction of a third monomer of formula (VIII)

In certain embodiments, the oxidized dextran comprises from about 0.1 to about 0.16, from about 0.11 to about 0.16, from about 0.12 to about 0.16, from about 0.13 to about 0.16, from about 0.14 to about 0.16, from about 0.15 to about 0.16, from about 0.1 to about 0.15, from about 0.1 to about 0.14, from about 0.1 to about 0.13, from about 0.1 to about 0.12, from about 0.1 to about 0.11, from about 0.11 to about 0.15, from about 0.11 to about 0.14, from about 0.11 to about 0.13, from about 0.11 to about 0.12, from about 0.12 to about 0.15, from about 0.12 to about 0.14, from about 0.12 to about 0.13, from about 0.13 to about 0.15, from about 0.13 to about 0.14, or from about 0.14 to about 0.15 mole fraction of a third monomer of formula (VIII). In certain embodiments, the oxidized dextran comprises from about 0.1 to about 0.16 mole fraction of a third monomer of formula (VIII). In certain embodiments, the oxidized dextran comprises from about 0.11 to about 0.14, about 0.12 to about 0.15, or about 0.13 to about 0.15 mole fraction of a third monomer of formula (VIII).

In certain embodiments, wherein the oxidized dextran has a Mw of from about 10 kDa to about 300 kDa, from about 10 kDa to about 200 kDa, from about 15 kDa to about 300 kDa, from about 15 kDa to about 200 kDa, from about 15 kDa to about 90 kDa, from about 15 kDa to about 80 kDa, from about 15 kDa to about 70 kDa, from about 15 kDa to about 80 kDa, from about 15 kDa to about 70 kDa, from about 15 kDa to about 60 kDa, from about 15 kDa to about 50 kDa, from about 15 kDa to about 40 kDa, from about 15 kDa to about 30 kDa, from about 15 kDa to about 25 kDa, from about 15 kDa to about 20 kDa, from about 20 kDa to about 90 kDa, from about 20 kDa to about 80 kDa, from about 20 kDa to about 70 kDa, from about 20 kDa to about 60 kDa, from about 20 kDa to about 70 kDa, from about 20 kDa to about 60 kDa, from about 20 kDa to about 50 kDa, from about 20 kDa to about 40 kDa, from about 20 kDa to about 30 kDa, from about 20 kDa to about 25 kDa, from about 25 kDa to about 90 kDa, from about 25 kDa to about 80 kDa, from about 25 kDa to about 70 kDa, from about 25 kDa to about 60 kDa, from about 25 kDa to about 70 kDa, from about 25 kDa to about 60 kDa, from about 25 kDa to about 50 kDa, from about 25 kDa to about 40 kDa, from about 25 kDa to about 30 kDa, from about 30 kDa to about 90 kDa, from about 30 kDa to about 80 kDa, from about 30 kDa to about 70 kDa, from about 30 kDa to about 60 kDa, from about 30 kDa to about 50 kDa, from about 30 kDa to about 40 kDa, from about 40 kDa to about 90 kDa, from about 40 kDa to about 80 kDa, from about 40 kDa to about 70 kDa, from about 40 kDa to about 60 kDa, from about 40 kDa to about 50 kDa, from about 50 kDa to about 90 kDa, from about 50 kDa to about 80 kDa, from about 50 kDa to about 70 kDa, from about 50 kDa to about 60 kDa, from about 60 kDa to about 90 kDa, from about 60 kDa to about 80 kDa, from about 60 kDa to about 70 kDa, from about 70 kDa to about 90 kDa, from about 70 kDa to about 80 kDa, or from about 80 kDa to about 90 kDa.

In certain embodiments, wherein the oxidized dextran has a Mw of from about 10 kDa to about 300 kDa. In certain embodiments, wherein the oxidized dextran has a Mw of from about 15 kDa to about 90 kDa. In certain embodiments, wherein the oxidized dextran has a Mw of from about 15 kDa to about 20 kDa, from about 15 kDa to about 25 kDa or from about 20 kDa to about 50 kDa.

In certain embodiments, the oxidized dextran has a Mn of from about 4 kDa to about 166 kDa, from about 4 kDa to about 100 kDa, from about 4 kDa to about 50 kDa, from about 4 kDa to about 40 kDa, from about 4 kDa to about 30 kDa, from about 4 kDa to about 20 kDa, from about 4 kDa to about 10 kDa, from about 4 kDa to about 9 kDa, from about 4 kDa to about 8 kDa, from about 4 kDa to about 7 kDa, from about 4 kDa to about 6 kDa, from about 4 kDa to about 5 kDa, from about 5 kDa to about 50 kDa, from about 5 kDa to about 40 kDa, from about 5 kDa to about 30 kDa, from about 5 kDa to about 20 kDa, from about 5 kDa to about 10 kDa, from about 5 kDa to about 9 kDa, from about 5 kDa to about 8 kDa, from about 5 kDa to about 7 kDa, from about 5 kDa to about 6 kDa, from about 6 kDa to about 50 kDa, from about 6 kDa to about 40 kDa, from about 6 kDa to about 30 kDa, from about 6 kDa to about 20 kDa, from about 6 kDa to about 10 kDa, from about 6 kDa to about 9 kDa, from about 6 kDa to about 8 kDa, from about 6 kDa to about 7 kDa, from about 7 kDa to about 50 kDa, from about 7 kDa to about 40 kDa, from about 7 kDa to about 30 kDa, from about 7 kDa to about 20 kDa, from about 7 kDa to about 10 kDa, from about 7 kDa to about 9 kDa, from about 7 kDa to about 8 kDa, from about 8 kDa to about 50 kDa, from about 8 kDa to about 40 kDa, from about 8 kDa to about 30 kDa, from about 8 kDa to about 20 kDa, from about 8 kDa to about 10 kDa, from about 8 kDa to about 9 kDa, from about 9 kDa to about 50 kDa, from about 9 kDa to about 40 kDa, from about 9 kDa to about 30 kDa, from about 9 kDa to about 20 kDa, from about 9 kDa to about 10 kDa, from about 10 kDa to about 50 kDa, from about 10 kDa to about 40 kDa, from about 10 kDa to about 30 kDa, from about 10 kDa to about 20 kDa, from about 20 kDa to about 50 kDa, from about 20 kDa to about 40 kDa, from about 20 kDa to about 30 kDa, from about 30 kDa to about 50 kDa, from about 30 kDa to about 40 kDa, or from about 40 kDa to about 50 kDa.

In certain embodiments, the oxidized dextran has a Mn of from about 4 kDa to about 166 kDa. In certain embodiments, the oxidized dextran has a Mn of from about 4 kDa to about 45 kDa. In certain embodiments, the oxidized dextran has a Mn of from about 4 kDa to about 6 kDa, from about 4 kDa to about 7 kDa, or from about 5 kDa to about 10 kDa.

In certain embodiments, the oxidized dextran has a polydispersity index (PDI) of from about 1.8 (Mw/Mn) to about 5.0 (Mw/Mn), from about 1.8 (Mw/Mn) to about 6.0 (Mw/Mn), from about 2.0 (Mw/Mn) to about 6.0 (Mw/Mn), from about 2.0 (Mw/Mn) to about 4.0 (Mw/Mn), from about 2.0 (Mw/Mn) to about 3.8 (Mw/Mn), from about 2.0 (Mw/Mn) to about 3.6 (Mw/Mn), from about 2.0 (Mw/Mn) to about 3.4 (Mw/Mn), from about 2.0 (Mw/Mn) to about 3.2 (Mw/Mn), from about 2.0 (Mw/Mn) to about 3.0 (Mw/Mn), from about 2.0 (Mw/Mn) to about 2.8 (Mw/Mn), from about 2.0 (Mw/Mn) to about 2.6 (Mw/Mn), from about 2.0 (Mw/Mn) to about 2.4 (Mw/Mn), from about 2.0 (Mw/Mn) to about 2.2 (Mw/Mn), from about 2.2 (Mw/Mn) to about 4.0 (Mw/Mn), from about 2.2 (Mw/Mn) to about 3.8 (Mw/Mn), from about 2.2 (Mw/Mn) to about 3.6 (Mw/Mn), from about 2.2 (Mw/Mn) to about 3.4 (Mw/Mn), from about 2.2 (Mw/Mn) to about 3.2 (Mw/Mn), from about 2.2 (Mw/Mn) to about 3.0 (Mw/Mn), from about 2.2 (Mw/Mn) to about 2.8 (Mw/Mn), from about 2.2 (Mw/Mn) to about 2.6 (Mw/Mn), from about 2.2 (Mw/Mn) to about 2.4 (Mw/Mn), from about 2.6 (Mw/Mn) to about 4.0 (Mw/Mn), from about 2.6 (Mw/Mn) to about 3.8 (Mw/Mn), from about 2.6 (Mw/Mn) to about 3.6 (Mw/Mn), from about 2.6 (Mw/Mn) to about 3.4 (Mw/Mn), from about 2.6 (Mw/Mn) to about 3.2 (Mw/Mn), from about 2.6 (Mw/Mn) to about 3.0 (Mw/Mn), from about 2.6 (Mw/Mn) to about 2.8 (Mw/Mn), from about 2.8 (Mw/Mn) to about 4.0 (Mw/Mn), from about 2.8 (Mw/Mn) to about 3.8 (Mw/Mn), from about 2.8 (Mw/Mn) to about 3.6 (Mw/Mn), from about 2.8 (Mw/Mn) to about 3.4 (Mw/Mn), from about 2.8 (Mw/Mn) to about 3.2 (Mw/Mn), from about 2.8 (Mw/Mn) to about 3.0 (Mw/Mn), from about 3.0 (Mw/Mn) to about 4.0 (Mw/Mn), from about 3.0 (Mw/Mn) to about 3.8 (Mw/Mn), from about 3.0 (Mw/Mn) to about 3.6 (Mw/Mn), from about 3.0 (Mw/Mn) to about 3.4 (Mw/Mn), from about 3.0 (Mw/Mn) to about 3.2 (Mw/Mn), from about 3.2 (Mw/Mn) to about 4.0 (Mw/Mn), from about 3.2 (Mw/Mn) to about 3.8 (Mw/Mn), from about 3.2 (Mw/Mn) to about 3.6 (Mw/Mn), from about 3.2 (Mw/Mn) to about 3.4 (Mw/Mn), from about 3.4 (Mw/Mn) to about 4.0 (Mw/Mn), from about 3.4 (Mw/Mn) to about 3.8 (Mw/Mn), from about 3.4 (Mw/Mn) to about 3.6 (Mw/Mn), from about 3.6 (Mw/Mn) to about 4.0 (Mw/Mn), from about 3.6 (Mw/Mn) to about 3.8 (Mw/Mn), or from about 3.8 (Mw/Mn) to about 4.0 (Mw/Mn).

In certain embodiments, the oxidized dextran has a polydispersity index (PDI) of from about 1.8 (Mw/Mn) to about 6.0 (Mw/Mn). In certain embodiments, the oxidized dextran has a polydispersity index (PDI) of from about 2.0 (Mw/Mn) to about 4.0 (Mw/Mn). In certain embodiments, the oxidized dextran has a polydispersity index (PDI) of from about 2.8 (Mw/Mn) to about 3.4 (Mw/Mn), from about 3.2 (Mw/Mn) to about 3.6 (Mw/Mn), or from about 3.4 (Mw/Mn) to about 4.0 (Mw/Mn).

In certain embodiments, the oxidized dextran has a Mz of from about 15 kDa to about 500 kDa, from about 20 kDa to about 450 kDa, from about 20 kDa to about 400 kDa, from about 20 kDa to about 300 kDa, from about 20 kDa to about 200 kDa, from about 20 kDa to about 100 kDa, from about 20 kDa to about 50 kDa, from about 20 kDa to about 45 kDa, from about 20 kDa to about 40 kDa, from about 20 kDa to about 35 kDa, from about 20 kDa to about 30 kDa, from about 20 kDa to about 25 kDa, from about 25 kDa to about 450 kDa, from about 25 kDa to about 400 kDa, from about 25 kDa to about 300 kDa, from about 25 kDa to about 200 kDa, from about 25 kDa to about 100 kDa, from about 25 kDa to about 50 kDa, from about 25 kDa to about 45 kDa, from about 25 kDa to about 40 kDa, from about 25 kDa to about 35 kDa, from about 25 kDa to about 30 kDa, from about 30 kDa to about 450 kDa, from about 30 kDa to about 400 kDa, from about 30 kDa to about 300 kDa, from about 30 kDa to about 200 kDa, from about 30 kDa to about 100 kDa, from about 30 kDa to about 50 kDa, from about 30 kDa to about 45 kDa, from about 30 kDa to about 40 kDa, from about 30 kDa to about 35 kDa, from about 35 kDa to about 450 kDa, from about 35 kDa to about 400 kDa, from about 35 kDa to about 300 kDa, from about 35 kDa to about 200 kDa, from about 35 kDa to about 100 kDa, from about 35 kDa to about 50 kDa, from about 35 kDa to about 45 kDa, from about 35 kDa to about 40 kDa, from about 40 kDa to about 450 kDa, from about 40 kDa to about 400 kDa, from about 40 kDa to about 300 kDa, from about 40 kDa to about 200 kDa, from about 40 kDa to about 100 kDa, from about 40 kDa to about 50 kDa, from about 40 kDa to about 45 kDa, from about 45 kDa to about 450 kDa, from about 45 kDa to about 400 kDa, from about 45 kDa to about 300 kDa, from about 45 kDa to about 200 kDa, from about 45 kDa to about 100 kDa, from about 45 kDa to about 50 kDa, from about 50 kDa to about 450 kDa, from about 50 kDa to about 400 kDa, from about 50 kDa to about 300 kDa, from about 50 kDa to about 200 kDa, from about 50 kDa to about 100 kDa, from about 100 kDa to about 450 kDa, from about 100 kDa to about 400 kDa, from about 100 kDa to about 300 kDa, from about 100 kDa to about 200 kDa, from about 200 kDa to about 450 kDa, 200 kDa to about 400 kDa, from about 200 kDa to about 300 kDa, from about 300 kDa to about 450 kDa, from about 300 kDa to about 400 kDa, or from about 400 kDa to about 450 kDa.

In certain embodiments, the oxidized dextran has a Mz of from about 15 kDa to about 500 kDa. In certain embodiments, the oxidized dextran has a Mz of from about 20 kDa to about 450 kDa. In certain embodiments, the oxidized dextran has a Mz of from about 20 kDa to about 35 kDa, about 30 kDa to about 45 kDa or about 40 kDa to about 100 kDa.

In certain embodiments, the oxidized dextran has a polydispersity index (PDI) of from about 1.5 (Mz/Mw) to about 6.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 5.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 4.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 3.5 (Mz/Mw), from about 1.5 (Mz/Mw) to about 3.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 2.5 (Mz/Mw), from about 1.5 (Mz/Mw) to about 2.0 (Mz/Mw), from about 2.0 (Mz/Mw) to about 5.0 (Mz/Mw), from about 2.0 (Mz/Mw) to about 4.0 (Mz/Mw), from about 2.0 (Mz/Mw) to about 3.5 (Mz/Mw), from about 2.0 (Mz/Mw) to about 3.0 (Mz/Mw), from about 2.0 (Mz/Mw) to about 2.5 (Mz/Mw), from about 2.5 (Mz/Mw) to about 5.0 (Mz/Mw), from about 2.5 (Mz/Mw) to about 4.0 (Mz/Mw), from about 2.5 (Mz/Mw) to about 3.5 (Mz/Mw), from about 2.5 (Mz/Mw) to about 3.0 (Mz/Mw), from about 3.0 (Mz/Mw) to about 5.0 (Mz/Mw), from about 3.0 (Mz/Mw) to about 4.0 (Mz/Mw), from about 3.0 (Mz/Mw) to about 3.5 (Mz/Mw), from about 3.5 (Mz/Mw) to about 5.0 (Mz/Mw), from about 3.5 (Mz/Mw) to about 4.0 (Mz/Mw), or from about 4.0 (Mz/Mw) to about 5.0 (Mz/Mw).

In certain embodiments, the oxidized dextran has a polydispersity index (PDI) of from about 1.5 (Mz/Mw) to about 6.0 (Mz/Mw). In certain embodiments, the oxidized dextran has a polydispersity index (PDI) of from about 1.5 (Mz/Mw) to about 5.0 (Mz/Mw). In certain embodiments, the oxidized dextran has a polydispersity index (PDI) of from about 1.5 (Mz/Mw) to about 2.0 (Mz/Mw), about 1.5 (Mz/Mw) to about 2.5 (Mz/Mw) or about 2.0 (Mz/Mw) to about 4.0 (Mz/Mw).

In certain embodiments, the oxidized dextran comprises a total amount of aldehyde groups of from about 0.5 to about 2.0, from about 0.5 to about 1.0, from about 0.6 to about 0.9, from about 0.6 to about 0.8, from about 0.6 to about 0.7, from about 0.7 to about 1.8, from about 0.7 to about 1.6, from about 0.7 to about 1.4, from about 0.7 to about 1.2, from about 0.7 to about 1.0, from about 0.7 to about 0.9, from about 0.7 to about 0.8, from about 0.8 to about 1.8, from about 0.8 to about 1.6, from about 0.8 to about 1.4, from about 0.8 to about 1.2, from about 0.8 to about 1.0, from about 0.8 to about 0.9, from about 0.9 to about 1.8, from about 0.9 to about 1.6, from about 0.9 to about 1.4, from about 0.9 to about 1.2, from about 0.9 to about 1.0, from about 1.0 to about 1.8, from about 1.0 to about 1.6, from about 1.0 to about 1.4, from about 1.0 to about 1.2, from about 1.2 to about 1.8, from about 1.2 to about 1.6, from about 1.2 to about 1.4, from about 1.4 to about 1.8, from about 1.4 to about 1.6, or from about 1.4 to about 1.8 mol/mol oxidized dextran. In certain embodiments, the oxidized dextran comprises a total amount of aldehyde groups of from about 0.5 to about 2.0 mol/mol oxidized dextran. In certain embodiments, the oxidized dextran comprises a total amount of aldehyde groups of from about 0.6 to about 0.9 mol/mol oxidized dextran. In certain embodiments, the oxidized dextran comprises a total amount of aldehyde groups of from about 0.6 to about 0.8, from about 0.7 to about 0.9, or from about 0.8 to about 1.4 mol/mol oxidized dextran.

In certain embodiments, the oxidized dextran comprises a total amount of primary aldehyde groups of from about 0.35 to about 2.0, about 0.35 to about 1.0, about 0.35 to about 0.7, about 0.35 to about 0.6, about 0.35 to about 0.55, about 0.35 to about 0.5, about 0.35 to about 0.45, about 0.35 to about 0.4, about 0.4 to about 1.5, about 0.4 to about 1.0, about 0.4 to about 0.6, about 0.4 to about 0.55, about 0.4 to about 0.5, about 0.4 to about 0.45, about 0.45 to about 1.5, about 0.45 to about 1.0, about 0.45 to about 0.7, about 0.45 to about 0.6, about 0.45 to about 0.55, about 0.45 to about 0.5, about 0.5 to about 1.5, about 0.5 to about 1.0, about 0.5 to about 0.7, about 0.5 to about 0.6, about 0.5 to about 0.55, about 0.55 to about 1.5, about 0.55 to about 1.0, about 0.55 to about 0.7, about 0.55 to about 0.6, about 0.6 to about 1.5, about 0.6 to about 1.0, about 0.6 to about 0.7, about 0.7 to about 1.5, about 0.7 to about 1.0, or about 1.0 to about 1.5 mol/mol oxidized dextran. In certain embodiments, the oxidized dextran comprises a total amount of primary aldehyde groups of from about 0.35 to about 2.0 mol/mol oxidized dextran. In certain embodiments, the oxidized dextran comprises a total amount of primary aldehyde groups of from about 0.35 to about 0.7 mol/mol oxidized dextran. In certain embodiments, the oxidized dextran comprises a total amount of primary aldehyde groups of from about 0.4 to about 0.55, from about 0.45 to about 0.6, or from about 0.55 to about 0.65 mol/mol oxidized dextran.

In certain embodiments, the oxidized dextran comprises a total amount of secondary aldehyde groups of from about 0.0 to about 1.3, from about 0.1 to about 1.0, from about 0.1 to about 0.7, from about 0.1 to about 0.5, from about 0.1 to about 0.4, from about 0.1 to about 0.3, from about 0.1 to about 0.2, from about 0.2 to about 1.0, from about 0.2 to about 0.7, from about 0.2 to about 0.5, from about 0.2 to about 0.4, from about 0.2 to about 0.3, from about 0.3 to about 1.0, from about 0.3 to about 0.7, from about 0.3 to about 0.5, from about 0.3 to about 0.4, from about 0.4 to about 1.0, from about 0.4 to about 0.7, from about 0.4 to about 0.5, from about 0.5 to about 1.0, from about 0.5 to about 0.7, or from about 0.7 to about 1.0 mol/mol oxidized dextran. In certain embodiments, the oxidized dextran comprises a total amount of secondary aldehyde groups of from about 0.0 to about 1.3 mol/mol oxidized dextran. In certain embodiments, the oxidized dextran comprises a total amount of secondary aldehyde groups of from about 0.1 to about 0.3 mol/mol oxidized dextran. In certain embodiments, the oxidized dextran comprises a total amount of secondary aldehyde groups of from about 0.1 to about 0.3, from about 0.2 to about 0.3, or from about 0.2 to about 0.5 mol/mol oxidized dextran.

In certain embodiments, the ratio of primary aldehyde groups to secondary aldehyde groups is from about 1.5 to about 6.0, from about 1.6 to about 6.0, from about 1.7 to about 6.0, from about 1.8 to about 6.0, from about 1.9 to about 6.0, from about 2.0 to about 6.0, from about 1.5 to about 4.0, from about 1.6 to about 4.0, from about 1.7 to about 4.0, from about 1.8 to about 4.0, from about 1.9 to about 4.0, from about 2.0 to about 4.0, from about 1.5 to about 3.5, from about 1.6 to about 3.5, from about 1.7 to about 3.5, from about 1.8 to about 3.5, from about 1.9 to about 3.5, from about 2.0 to about 3.5, from about 1.5 to about 3.25, from about 1.6 to about 3.25, from about 1.7 to about 3.25, from about 1.8 to about 3.25, from about 1.9 to about 3.25, from about 2.0 to about 3.5, from about 1.5 to about 3.0, from about 1.6 to about 3.0, from about 1.7 to about 3.0, from about 1.8 to about 3.0, from about 1.9 to about 3.0, from about 2.0 to about 3.0, from about 1.5 to about 2.75, from about 1.6 to about 2.75, from about 1.7 to about 2.75, from about 1.8 to about 2.75, from about 1.9 to about 2.75, from about 2.0 to about 2.75, from about 1.5 to about 2.5, from about 1.6 to about 2.5, from about 1.7 to about 2.5, from about 1.8 to about 2.5, from about 1.9 to about 2.5, from about 2.0 to about 2.5, from about 1.5 to about 2.25, from about 1.6 to about 2.25, from about 1.7 to about 2.25, from about 1.8 to about 2.25, from about 1.9 to about 2.25, from about 2.0 to about 2.25, from about 1.5 to about 2.0, from about 1.6 to about 2.0, from about 1.7 to about 2.0, from about 1.8 to about 2.0, from about 1.9 to about 2.0, from about 2.25 to about 3.5, from about 2.25 to about 3.25, from about 2.25 to about 3.0, from about 2.25 to about 2.75, from about 2.25 to about 2.5, from about 2.5 to about 3.5, from about 2.5 to about 3.25, from about 2.5 to about 3.0, from about 2.5 to about 2.75, from about 2.75 to about 3.5, from about 2.75 to about 3.25, from about 2.75 to about 3.0, from about 3.0 to about 3.5, from about 3.0 to about 3.25, or from about 3.25 to about 3.5. In certain embodiments, the ratio of primary aldehyde groups to secondary aldehyde groups is from about 1.5 to about 6.0. In certain embodiments, the ratio of primary aldehyde groups to secondary aldehyde groups is from about 1.8 to about 6.0 or from about 1.8 to about 3.5. In certain embodiments, the ratio of primary aldehyde groups to secondary aldehyde groups is from about 1.8 to about 2.0, about 1.8 to about 2.25, or about 2.0 to about 3.25.

In certain embodiments, the degree of oxidation is from about 25% to about 100%, from about 25% to about 90%, from about 25% to about 80%, from about 25% to about 70%, from about 25% to about 60%, from about 30% to about 45%, from about 30% to about 40%, from about 30% to about 35%, from about 35% to about 45%, from about 35% to about 40%. In certain embodiments, the degree of oxidation is from about 25% to about 100% or from about 30% to about 50%. In certain embodiments, the degree of oxidation is from about 30% to about 45%, or about 35% to about 45%.

In certain embodiments, the oxidized dextran composition comprises about 1% (w/w), about 2% (w/w), about 3% (w/w), about 4% (w/w), about 5% (w/w), about 6% (w/w), about 7% (w/w), about 8% (w/w), about 9% (w/w), about 10% (w/w), about 11% (w/w), about 12% (w/w), about 13% (w/w), about 14% (w/w), about 15% (w/w), about 16% (w/w), about 17% (w/w), about 18% (w/w), about 19% (w/w), about 20% (w/w), about 21% (w/w), about 22% (w/w), about 23% (w/w), about 24% (w/w), or about 25% (w/w) by weight of the total weight of the solution.

In certain embodiments, the oxidized dextran composition comprises from about 1% (w/w) to about 25% (w/w), from about 1% (w/w) to about 20% (w/w), from about 1% (w/w) to about 15% (w/w), from about 1% (w/w) to about 10% (w/w), from about 1% (w/w) to about 9% (w/w), from about 1% (w/w) to about 8% (w/w), from about 1% (w/w) to about 7% (w/w), from about 1% (w/w) to about 6% (w/w), from about 1% (w/w) to about 5% (w/w), from about 1% (w/w) to about 4% (w/w), from about 1% (w/w) to about 3% (w/w), from about 1% (w/w) to about 2% (w/w), from about 2% (w/w) to about 10% (w/w), from about 2% (w/w) to about 9% (w/w), from about 2% (w/w) to about 8% (w/w), from about 2% (w/w) to about 7% (w/w), from about 2% (w/w) to about 6% (w/w), from about 2% (w/w) to about 5% (w/w), from about 2% (w/w) to about 4% (w/w), from about 2% (w/w) to about 3% (w/w), from about 3% (w/w) to about 10% (w/w), from about 3% (w/w) to about 9% (w/w), from about 3% (w/w) to about 8% (w/w), from about 3% (w/w) to about 7% (w/w), from about 3% (w/w) to about 6% (w/w), from about 3% (w/w) to about 5% (w/w), from about 3% (w/w) to about 4% (w/w), from about 4% (w/w) to about 10% (w/w), from about 4% (w/w) to about 9% (w/w), from about 4% (w/w) to about 8% (w/w), from about 4% (w/w) to about 7% (w/w), from about 4% (w/w) to about 6% (w/w), from about 4% (w/w) to about 5% (w/w), from about 5% (w/w) to about 10% (w/w), from about 5% (w/w) to about 9% (w/w), from about 5% (w/w) to about 8% (w/w), from about 5% (w/w) to about 7% (w/w), from about 5% (w/w) to about 6% (w/w), from about 6% (w/w) to about 10% (w/w), from about 6% (w/w) to about 9% (w/w), from about 6% (w/w) to about 8% (w/w), from about 6% (w/w) to about 7% (w/w), from about 7% (w/w) to about 10% (w/w), from about 7% (w/w) to about 9% (w/w), from about 7% (w/w) to about 8% (w/w), from about 8% (w/w) to about 10% (w/w), from about 8% (w/w) to about 9% (w/w), or from about 9% (w/w) to about 10% (w/w) of the oxidized dextran. In certain embodiments, the oxidized dextran composition comprises from about 1% (w/w) to about 25% (w/w) or from about 1% (w/w) to about 10% (w/w) of the oxidized dextran. In certain embodiments, the oxidized dextran composition comprises from about 2% (w/w) to about 5% (w/w), from about 4% (w/w) to about 7% (w/w), or from about 6% (w/w) to about 10% (w/w) of the oxidized dextran.

In certain embodiments, the oxidized dextran composition has a viscosity of from about 1.0 cP to about 2,000 cP, from about 1.0 cP to about 1,000 cP, from about 1.0 cP to about 100 cP, from about 1.0 cP to about 10 cP, from about 1.0 cP to about 9 cP, from about 1.0 cP to about 8 cP, from about 1.0 cP to about 7 cP, from about 1.0 cP to about 6 cP, from about 1.0 cP to about 5 cP, from about 1.0 cP to about 4 cP, from about 1.0 cP to about 3 cP, from about 1.0 cP to about 2 cP, from about 2.0 cP to about 10.0 cP, from about 2.0 cP to about 9.0 cP, from about 2.0 cP to about 8.0 cP, from about 2.0 cP to about 7.0 cP, from about 2.0 cP to about 6.0 cP, from about 2.0 cP to about 5.0 cP, from about 2.0 cP to about 4.0 cP, from about 2.0 cP to about 3.0 cP, from about 3.0 cP to about 10.0 cP, from about 3.0 cP to about 9.0 cP, from about 3.0 cP to about 8.0 cP, from about 3.0 cP to about 7.0 cP, from about 3.0 cP to about 6.0 cP, from about 3.0 cP to about 5.0 cP, from about 3.0 cP to about 4.0 cP, from about 4.0 cP to about 10.0 cP, from about 4.0 cP to about 9.0 cP, from about 4.0 cP to about 8.0 cP, from about 4.0 cP to about 7.0 cP, from about 4.0 cP to about 6.0 cP, from about 4.0 cP to about 5.0 cP, from about 5.0 cP to about 10.0 cP, from about 5.0 cP to about 9.0 cP, from about 5.0 cP to about 8.0 cP, from about 5.0 cP to about 7.0 cP, from about 5.0 cP to about 6.0 cP, from about 6.0 cP to about 10.0 cP, from about 6.0 cP to about 9.0 cP, from about 6.0 cP to about 8.0 cP, from about 6.0 cP to about 7.0 cP, from about 7.0 cP to about 10.0 cP, from about 7.0 cP to about 9.0 cP, from about 7.0 cP to about 8.0 cP, from about 8.0 cP to about 10.0 cP, from about 8.0 cP to about 9.0 cP, or from about 9.0 cP to about 10.0 cP.

In certain embodiments, the oxidized dextran composition has a viscosity of from about 1 cP to about 2,000 cP, or from about 1 cP to about 10 cP. In certain embodiments, the oxidized dextran composition has a viscosity of from about 1.0 cP to about 3.0 cP, from about 1.0 cP to about 5.0 cP, or from about 3.0 cP to about 9.0 cP.

In certain embodiments, the oxidized dextran composition has a pH of from about 5.0 to about 7.5, from about 5.2 to about 7.5, from about 5.4 to about 7.5, from about 5.6 to about 7.5, from about 5.8 to about 7.5, from about 6.0 to about 7.5, from about 6.2 to about 7.5, from about 6.4 to about 7.5, from about 6.6 to about 7.5, from about 6.8 to about 7.5, from about 7.0 to about 7.5, from about 5.0 to about 7.0, from about 5.0 to about 6.8, from about 5.0 to about 6.6, from about 5.0 to about 6.4, from about 5.0 to about 6.2, from about 5.0 to about 6.0, from about 5.0 to about 5.8, from about 5.0 to about 5.6, from about 5.0 to about 5.4, from about 5.0 to about 5.2, from about 5.2 to about 7.0, from about 5.2 to about 6.8, from about 5.2 to about 6.6, from about 5.2 to about 6.4, from about 5.2 to about 6.2, from about 5.2 to about 6.0, from about 5.2 to about 5.8, from about 5.2 to about 5.6, from about 5.2 to about 5.4, from about 5.4 to about 7.0, from about 5.4 to about 6.8, from about 5.4 to about 6.6, from about 5.4 to about 6.4, from about 5.4 to about 6.2, from about 5.4 to about 6.0, from about 5.4 to about 5.8, from about 5.4 to about 5.6, from about 5.6 to about 7.0, from about 5.6 to about 6.8, from about 5.6 to about 6.6, from about 5.6 to about 6.4, from about 5.6 to about 6.2, from about 5.6 to about 6.0, from about 5.6 to about 5.8, from about 5.8 to about 7.0, from about 5.8 to about 6.8, from about 5.8 to about 6.6, from about 5.8 to about 6.4, from about 5.8 to about 6.2, from about 5.8 to about 6.0, from about 6.0 to about 7.0, from about 6.0 to about 6.8, from about 6.0 to about 6.6, from about 6.0 to about 6.4, from about 6.0 to about 6.2, from about 6.2 to about 7.0, from about 6.2 to about 6.8, from about 6.2 to about 6.6, from about 6.2 to about 6.4, from about 6.4 to about 7.0, from about 6.4 to about 6.8, from about 6.4 to about 6.6, from about 6.6 to about 7.0, from about 6.6 to about 6.8, or from about 6.8 to about 7.0. In certain embodiments, the oxidized dextran composition has a pH of from about 5.0 to about 7.5. In certain embodiments, the oxidized dextran composition has a pH of from about 5.0 to about 6.0, from about 5.0 to about 6.8, or from about 5.6 to about 7.0.

In certain embodiments, the oxidized dextran composition has a conductivity of from about 0.05 (mS/cm) to about 1.7 (mS/cm), from about 0.05 (mS/cm) to about 1.2 (mS/cm), from about 0.05 (mS/cm) to about 0.7 (mS/cm), from about 0.05 (mS/cm) to about 0.5 (mS/cm), from about 0.05 (mS/cm) to about 0.3 (mS/cm), from about 0.05 (mS/cm) to about 0.25 (mS/cm), from about 0.05 (mS/cm) to about 0.2 (mS/cm), from about 0.05 (mS/cm) to about 0.15 (mS/cm), from about 0.05 (mS/cm) to about 0.1 (mS/cm), from about 0.1 (mS/cm) to about 0.7 (mS/cm), from about 0.1 (mS/cm) to about 0.5 (mS/cm), from about 0.1 (mS/cm) to about 0.3 (mS/cm), from about 0.1 (mS/cm) to about 0.25 (mS/cm), from about 0.1 (mS/cm) to about 0.2 (mS/cm), from about 0.1 (mS/cm) to about 0.15 (mS/cm), from about 0.15 (mS/cm) to about 0.7 (mS/cm), from about 0.15 (mS/cm) to about 0.5 (mS/cm), from about 0.15 (mS/cm) to about 0.3 (mS/cm), from about 0.15 (mS/cm) to about 0.25 (mS/cm), from about 0.15 (mS/cm) to about 0.2 (mS/cm), from about 0.2 (mS/cm) to about 0.7 (mS/cm), from about 0.2 (mS/cm) to about 0.5 (mS/cm), from about 0.2 (mS/cm) to about 0.3 (mS/cm), from about 0.2 (mS/cm) to about 0.25 (mS/cm), from about 0.25 (mS/cm) to about 0.7 (mS/cm), from about 0.25 (mS/cm) to about 0.5 (mS/cm), from about 0.25 (mS/cm) to about 0.3 (mS/cm), from about 0.3 (mS/cm) to about 0.7 (mS/cm), from about 0.3 (mS/cm) to about 0.5 (mS/cm), or from about 0.5 (mS/cm) to about 0.7 (mS/cm).

In certain embodiments, the oxidized dextran composition has a conductivity of from about 0.05 (mS/cm) to about 1.7 (mS/cm). In certain embodiments, the oxidized dextran composition has a conductivity of from about 0.05 (mS/cm) to about 0.7 (mS/cm). In certain embodiments, the oxidized dextran composition has a conductivity of from about 0.1 (mS/cm) to about 0.3 (mS/cm), from about 0.2 (mS/cm) to about 0.5 (mS/cm) or from about 0.3 (mS/cm) to about 0.7 (mS/cm).

In certain embodiments, the oxidized dextran has two or more properties selected from a Mw of from about 10 kDa to about 300 kDa, a Mn of from about 4 kDa to about 166 kDa, a PDI of from about 1.8 to about 6.0 (Mw/Mn), a total amount of aldehyde groups of from about 0.5 to about 2.0 mol aldehydes/mol oxidized dextran, a total amount of primary aldehydes of from about 0.35 to about 2.0 mol aldehydes/mol oxidized dextran, a total amount of secondary aldehydes of from about 0.0 to about 1.3 mol aldehydes/mol oxidized dextran, a ratio of primary aldehyde groups to secondary aldehyde groups from about 1.6 to about 6.0, a degree of oxidation from about 25% to about 100%.

In certain embodiments, the oxidized dextran composition comprises a plurality (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12) or all of the following features: (i) a Mw of from about 15 kDa to about 90 kDa, (ii) a Mn of from about 4 kDa to about 45 kDa, (iii) a Mz of from about 22 kDa to about 450 kDa, (iv) a PDI (Mw/Mn) of from about 2.0 to about 4.0, (v) a PDI (Mz/Mw) of from about 1.5 to about 5.0, (vi) a mole fraction of the monomer of formula (V) of from about 0.5 to about 0.7, (vii) a mole fraction of the monomer of formula (VI) and/or the monomer of formula (VII) of from about 0.15 to about 0.35, (viii) a mole fraction of the monomer of formula (VIII) of from about 0.1 to about 0.16, (ix) a total amount of aldehyde groups of from about 0.6 to about 0.9 mol aldehydes/mol oxidized dextran, (x) a total amount of primary aldehyde groups of from about 0.38 to about 0.7 mol aldehydes/mol oxidized dextran, (xi) a total amount of secondary aldehyde groups of from about 0.1 to about 0.31 mol aldehydes/mol oxidized dextran, (xii) a ratio of primary aldehyde groups to secondary aldehyde groups of from about 1.8 to about 3.5, and (xiii) a degree of oxidation of from about 32% to about 45%.

In certain embodiments, the oxidized dextran composition comprises a plurality (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, or 16) or all of the following features: (i) a Mw of from about 15 kDa to about 90 kDa, (ii) a Mn of from about 4 kDa to about 45 kDa, (iii) a Mz of from about 22 kDa to about 450 kDa, (iv) a PDI (Mw/Mn) of from about 2.0 to about 4.0, (v) a PDI (Mz/Mw) of from about 1.5 to about 5.0, (vi) a mole fraction of the monomer of formula (V) of from about 0.5 to about 0.7, (vii) a mole fraction of the monomer of formula (VI) and/or the monomer of formula (VII) of from about 0.15 to about 0.35, (viii) a mole fraction of the monomer of formula (VIII) of from about 0.1 to about 0.16, (ix) a total amount of aldehyde groups of from about 0.6 to about 0.9 mol aldehydes/mol oxidized dextran, (x) a total amount of primary aldehyde groups of from about 0.38 to about 0.7 mol aldehydes/mol oxidized dextran, (xi) a total amount of secondary aldehyde groups of from about 0.1 to about 0.31 mol aldehydes/mol oxidized dextran, (xii) a ratio of primary aldehyde groups to secondary aldehyde groups of from about 1.8 to about 3.5, (xiii) a degree of oxidation of from about 32% to about 45%, (xiv) a concentration of the acrylated chitosan in an aqueous medium or from about 1% (w/w) to about 10% (w/w), (xv) a viscosity of from about 1 cP to about 10 cP, (xvi) a pH of from about 5.0 to about 7.5, and (xvii) a conductivity of from about 0.05 mS/cm to about 0.7 mS/cm.

V Methods of Making Oxidized Dextran Compositions

Dextran is an α-D-1,6-glucose-linked glucan with side chains 1-3 linked to the backbone units of the dextran biopolymer.

One aspect of the invention provides methods of preparing oxidized dextran compositions. In various embodiments, the methods generally include:

-   -   (a) contacting a solution comprising a raw dextran material with         an oxidizing agent to form an oxidized dextran intermediate,         wherein the concentration of the raw dextran material in the         solution is greater than 1% (w/w); and     -   (b) purifying the oxidized dextran intermediate to produce an         oxidized dextran composition.

In certain embodiments, the oxidized dextran composition produced in step (b) is the oxidized dextran composition described herein.

In certain embodiments, during step (a), the concentration of the raw dextran material in the aqueous solution is at least 1.1% (w/w), 1.2% (w/w), 1.3% (w/w), 1.4% (w/w), 1.5% (w/w), 1.6% (w/w), 1.7% (w/w), 1.8% (w/w), 1.9% (w/w), or 2.0% (w/w) or greater. In certain embodiments, during step (a), the concentration of the raw dextran material in the aqueous solution is at least 1.1% (w/w).

In certain embodiments, during step (a), the raw dextran material has a Mw of from about 50 kDa to about 2,000 kDa, from about 50 kDa to about 1,000 kDa, from about 50 kDa to about 500 kDa, from about 50 kDa to about 400 kDa, from about 50 kDa to about 300 kDa, from about 50 kDa to about 200 kDa, from about 50 kDa to about 120 kDa, from about 60 kDa to about 2,000 kDa, from about 60 kDa to about 1,000 kDa, from about 60 kDa to about 500 kDa, from about 60 kDa to about 400 kDa, from about 60 kDa to about 300 kDa, from about 60 kDa to about 200 kDa, from about 60 kDa to about 120 kDa, from about 60 kDa to about 100 kDa, from about 60 kDa to about 90 kDa, from about 60 kDa to about 80 kDa, from about 60 kDa to about 70 kDa, from about 70 kDa to about 400 kDa, from about 70 kDa to about 300 kDa, from about 70 kDa to about 200 kDa, from about 70 kDa to about 120 kDa, from about 70 kDa to about 100 kDa, from about 70 kDa to about 90 kDa, from about 70 kDa to about 80 kDa, from about 80 kDa to about 400 kDa, from about 80 kDa to about 300 kDa, from about 80 kDa to about 200 kDa, from about 80 kDa to about 120 kDa, from about 80 kDa to about 100 kDa, from about 80 kDa to about 90 kDa, from about 90 kDa to about 400 kDa, from about 90 kDa to about 300 kDa, from about 90 kDa to about 200 kDa, from about 90 kDa to about 120 kDa, from about 90 kDa to about 100 kDa, from about 100 kDa to about 400 kDa, from about 100 kDa to about 300 kDa, from about 100 kDa to about 200 kDa, from about 100 kDa to about 120 kDa, from about 120 kDa to about 400 kDa, from about 120 kDa to about 300 kDa, from about 120 kDa to about 200 kDa, from about 200 kDa to about 400 kDa, from about 200 kDa to about 300 kDa, or from about 300 kDa to about 400 kDa. In certain embodiments, during step (a), the raw dextran material has a Mw of from about 50 kDa to about 2,000 kDa. In certain embodiments, during step (a), the raw dextran material has a Mw of from about 60 kDa to about 400 kDa. In certain embodiments, during step (a), the raw dextran material has a Mw of from about 60 kDa to about 100 kDa, from about 80 kDa to about 200 kDa, from about 100 kDa to about 120 kDa, or from about 100 kDa to about 400 kDa. In certain embodiments, during step (a), the raw dextran material has a Mw of from about 80 kDa to about 200 kDa. In certain embodiments, during step (a), the raw dextran material has a Mw of from about 100 kDa to about 120 kDa.

In certain embodiments, during step (a), the raw dextran material has a Mn of from about 15 kDa to about 500 kDa, from about 15 kDa to about 250 kDa, from about 25 kDa to about 500 kDa, from about 25 kDa to about 250 kDa, from about 25 kDa to about 200 kDa, from about 25 kDa to about 160 kDa, from about 25 kDa to about 140 kDa, from about 25 kDa to about 120 kDa, from about 25 kDa to about 100 kDa, from about 25 kDa to about 90 kDa, from about 25 kDa to about 80 kDa, from about 25 kDa to about 70 kDa, from about 25 kDa to about 60 kDa, from about 25 kDa to about 50 kDa, from about 25 kDa to about 40 kDa, from about 25 kDa to about 35 kDa, from about 25 kDa to about 30 kDa, from about 30 kDa to about 250 kDa, from about 30 kDa to about 200 kDa, from about 30 kDa to about 160 kDa, from about 30 kDa to about 140 kDa, from about 30 kDa to about 120 kDa, from about 30 kDa to about 100 kDa, from about 30 kDa to about 90 kDa, from about 30 kDa to about 80 kDa, from about 30 kDa to about 70 kDa, from about 30 kDa to about 60 kDa, from about 30 kDa to about 50 kDa, from about 30 kDa to about 40 kDa, from about 30 kDa to about 35 kDa, from about 35 kDa to about 250 kDa, from about 35 kDa to about 200 kDa, from about 35 kDa to about 160 kDa, from about 35 kDa to about 140 kDa, from about 35 kDa to about 120 kDa, from about 35 kDa to about 100 kDa, from about 35 kDa to about 90 kDa, from about 35 kDa to about 80 kDa, from about 35 kDa to about 70 kDa, from about 35 kDa to about 60 kDa, from about 35 kDa to about 50 kDa, from about 35 kDa to about 40 kDa, from about 40 kDa to about 250 kDa, from about 40 kDa to about 200 kDa, from about 40 kDa to about 160 kDa, from about 40 kDa to about 140 kDa, from about 40 kDa to about 120 kDa, from about 40 kDa to about 100 kDa, from about 40 kDa to about 90 kDa, from about 40 kDa to about 80 kDa, from about 40 kDa to about 70 kDa, from about 40 kDa to about 60 kDa, from about 40 kDa to about 50 kDa, from about 50 kDa to about 250 kDa, from about 50 kDa to about 200 kDa, from about 50 kDa to about 160 kDa, from about 50 kDa to about 150 kDa, from about 50 kDa to about 120 kDa, from about 50 kDa to about 100 kDa, from about 50 kDa to about 90 kDa, from about 50 kDa to about 80 kDa, from about 50 kDa to about 70 kDa, or from about 50 kDa to about 60 kDa.

In certain embodiments, during step (a), the raw dextran material has a Mn of from about 15 kDa to about 500 kDa. In certain embodiments, during step (a), the raw dextran material has a Mn of from about 25 kDa to about 250 kDa. In certain embodiments, during step (a), the raw dextran material has a Mn of from about 25 kDa to about 120 kDa, from about 40 kDa to about 140 kDa, from about 50 kDa to about 80 kDa, or from about 80 kDa to about 200 kDa. In certain embodiments, during step (a), the raw dextran material has a Mn of from about 25 kDa to about 140 kDa. In certain embodiments, during step (a), the raw dextran material has a Mn of from about 50 kDa to about 80 kDa.

In certain embodiments, during step (a), the raw dextran material has a PDI of from about 1.3 (Mw/Mn) to about 5.0 (Mw/Mn), from about 1.4 (Mw/Mn) to about 5.0 (Mw/Mn), from about 1.4 (Mw/Mn) to about 4.0 (Mw/Mn), from about 1.4 (Mw/Mn) to about 3.0 (Mw/Mn), from about 1.5 (Mw/Mn) to about 5.0 (Mw/Mn), from about 1.5 (Mw/Mn) to about 4.5 (Mw/Mn), from about 1.5 (Mw/Mn) to about 4.0 (Mw/Mn), from about 1.5 (Mw/Mn) to about 3.0 (Mw/Mn), from about 1.5 (Mw/Mn) to about 2.5 (Mw/Mn), from about 1.5 (Mw/Mn) to about 2.0 (Mw/Mn), from about 1.5 (Mw/Mn) to about 1.9 (Mw/Mn), from about 1.5 (Mw/Mn) to about 1.7 (Mw/Mn), from about 1.7 (Mw/Mn) to about 3.0 (Mw/Mn), from about 1.7 (Mw/Mn) to about 2.5 (Mw/Mn), from about 1.7 (Mw/Mn) to about 2.0 (Mw/Mn), from about 1.7 (Mw/Mn) to about 1.9 (Mw/Mn), from about 1.9 (Mw/Mn) to about 3.0 (Mw/Mn), from about 1.9 (Mw/Mn) to about 2.5 (Mw/Mn), or from about 1.9 (Mw/Mn) to about 2.0 (Mw/Mn).

In certain embodiments, during step (a), the raw dextran material has a PDI of from about 1.4 (Mw/Mn) to about 5.0 (Mw/Mn). In certain embodiments, during step (a), the raw dextran material has a PDI of from about 1.5 (Mw/Mn) to about 5.0 (Mw/Mn). In certain embodiments, during step (a), the raw dextran material has a PDI of from about 1.5 (Mw/Mn) to about 4.5 (Mw/Mn). In certain embodiments, during step (a), the raw dextran material has a PDI of from about 1.5 (Mw/Mn) to about 3.0 (Mw/Mn). In certain embodiments, during step (a), the raw dextran material has a PDI of from about 1.5 (Mw/Mn) to about 2.0 (Mw/Mn), from about 1.5 (Mw/Mn) to about 2.5 (Mw/Mn), or from about 1.9 (Mw/Mn) to about 3.0 (Mw/Mn). In certain embodiments, during step (a), the raw dextran material has a PDI of from about 1.5 (Mw/Mn) to about 2.0 (Mw/Mn).

In certain embodiments, during step (a), the raw dextran material has a Mz of from about 250 kDa to about 5,000 kDa, from about 250 kDa to about 4,000 kDa, from about 250 kDa to about 3,000 kDa, from about 250 kDa to about 2,000 kDa, from about 300 kDa to about 5,000 kDa, from about 300 kDa to about 4,000 kDa, from about 300 kDa to about 3,000 kDa, about 300 kDa to about 2,000 kDa, from about 300 kDa to about 1,500 kDa, from about 300 kDa to about 1,200 kDa, from about 300 kDa to about 1,000 kDa, from about 300 kDa to about 750 kDa, from about 300 kDa to about 500 kDa, from about 300 kDa to about 450 kDa, from about 300 kDa to about 400 kDa, from about 300 kDa to about 350 kDa, from about 350 kDa to about 2,000 kDa, from about 350 kDa to about 1,500 kDa, from about 350 kDa to about 1,200 kDa, from about 350 kDa to about 1,000 kDa, from about 350 kDa to about 750 kDa, from about 350 kDa to about 500 kDa, from about 350 kDa to about 450 kDa, from about 350 kDa to about 400 kDa, from about 400 kDa to about 2,000 kDa, from about 400 kDa to about 1,500 kDa, from about 400 kDa to about 1,200 kDa, from about 400 kDa to about 1,000 kDa, from about 400 kDa to about 750 kDa, from about 400 kDa to about 500 kDa, from about 400 kDa to about 450 kDa, from about 450 kDa to about 2,000 kDa, from about 450 kDa to about 1,500 kDa, from about 450 kDa to about 1,200 kDa, from about 450 kDa to about 1,000 kDa, from about 450 kDa to about 750 kDa, from about 450 kDa to about 500 kDa, from about 500 kDa to about 2,000 kDa, from about 500 kDa to about 1,500 kDa, from about 500 kDa to about 1,200 kDa, from about 500 kDa to about 1,000 kDa, from about 500 kDa to about 750 kDa, from about 750 kDa to about 2,000 kDa, from about 750 kDa to about 1,500 kDa, from about 750 kDa to about 1,200 kDa, from about 750 kDa to about 1,000 kDa, from about 1,000 kDa to about 2,000 kDa, from about 1,000 kDa to about 1,500 kDa, from about 1,000 kDa to about 1,200 kDa, from about 1,200 kDa to about 2,000 kDa, from about 1,200 kDa to about 1,500 kDa, or from about 1,500 kDa to about 2,000 kDa.

In certain embodiments, during step (a), the raw dextran material has a Mz of from about 250 kDa to about 5,000 kDa. In certain embodiments, during step (a), the raw dextran material has a Mz of from about 300 kDa to about 2,000 kDa. In certain embodiments, during step (a), the raw dextran material has a Mz of from about 300 kDa to about 1,000 kDa, from about 350 kDa to about 1,500 kDa, from about 400 kDa to about 1,200 kDa, or from about 500 kDa to about 2,000 kDa. In certain embodiments, during step (a), the raw dextran material has a Mz of from about 350 kDa to about 1,500 kDa. In certain embodiments, during step (a), the raw dextran material has a Mz of from about 400 kDa to about 1,200 kDa.

In certain embodiments, during step (a), the raw dextran material has a PDI of from about 1.4 (Mz/Mw) to about 15.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 15.0 (Mz/Mw), from about 1.7 (Mz/Mw) to about 15.0 (Mz/Mw), from about 2.0 (Mz/Mw) to about 15.0 (Mz/Mw), from about 3.0 (Mz/Mw) to about 15.0 (Mz/Mw), from about 6.0 (Mz/Mw) to about 15.0 (Mz/Mw), from about 9.0 (Mz/Mw) to about 15.0 (Mz/Mw), from about 12.0 (Mz/Mw) to about 15.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 12.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 9.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 6.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 5.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 4.5 (Mz/Mw), from about 1.5 (Mz/Mw) to about 3.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 2.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 1.7 (Mz/Mw), from about 1.7 (Mz/Mw) to about 12.0 (Mz/Mw), from about 1.7 (Mz/Mw) to about 9.0 (Mz/Mw), from about 1.7 (Mz/Mw) to about 6.0 (Mz/Mw), from about 1.7 (Mz/Mw) to about 5.0 (Mz/Mw), from about 1.7 (Mz/Mw) to about 4.5 (Mz/Mw), from about 1.7 (Mz/Mw) to about 3.0 (Mz/Mw), from about 1.7 (Mz/Mw) to about 2.0 (Mz/Mw), from about 2.0 (Mz/Mw) to about 12.0 (Mz/Mw), from about 2.0 (Mz/Mw) to about 9.0 (Mz/Mw), from about 2.0 (Mz/Mw) to about 6.0 (Mz/Mw), from about 2.0 (Mz/Mw) to about 5.0 (Mz/Mw), from about 2.0 (Mz/Mw) to about 4.5 (Mz/Mw), from about 2.0 (Mz/Mw) to about 3.0 (Mz/Mw), from about 3.0 (Mz/Mw) to about 12.0 (Mz/Mw), from about 3.0 (Mz/Mw) to about 9.0 (Mz/Mw), from about 3.0 (Mz/Mw) to about 6.0 (Mz/Mw), from about 3.0 (Mz/Mw) to about 5.0 (Mz/Mw), from about 3.0 (Mz/Mw) to about 4.5 (Mz/Mw), from about 4.5 (Mz/Mw) to about 12.0 (Mz/Mw), from about 4.5 (Mz/Mw) to about 9.0 (Mz/Mw), from about 4.5 (Mz/Mw) to about 6.0 (Mz/Mw), from about 4.5 (Mz/Mw) to about 5.0 (Mz/Mw), from about 5.0 (Mz/Mw) to about 12.0 (Mz/Mw), from about 5.0 (Mz/Mw) to about 9.0 (Mz/Mw), from about 5.0 (Mz/Mw) to about 6.0 (Mz/Mw), from about 6.0 (Mz/Mw) to about 12.0 (Mz/Mw), from about 6.0 (Mz/Mw) to about 9.0 (Mz/Mw), or from about 9.0 (Mz/Mw) to about 12.0 (Mz/Mw).

In certain embodiments, during step (a), the raw dextran material has a PDI of from about 1.4 (Mz/Mw) to about 15.0 (Mz/Mw). In certain embodiments, during step (a), the raw dextran material has a PDI of from about 1.5 (Mz/Mw) to about 15.0 (Mz/Mw). In certain embodiments, during step (a), the raw dextran material has a PDI of from about 1.5 (Mz/Mw) to about 9.0 (Mz/Mw), from about 1.5 (Mz/Mw) to about 12.0 (Mz/Mw), from about 3.0 (Mz/Mw) to about 12.0 (Mz/Mw), or from about 6.0 (Mz/Mw) to about 15.0 (Mz/Mw). In certain embodiments, during step (a), the raw dextran material has a PDI of from about 1.5 (Mz/Mw) to about 12.0 (Mz/Mw). In certain embodiments, during step (a), the raw dextran material has a PDI of from about 3.0 (Mz/Mw) to about 12.0 (Mz/Mw).

In certain embodiments, the raw dextran material comprises two or more of the features selected from an Mw of from about 50 kDa to about 2,000 kDa, an Mn of from about 15 kDa to about 500 kDa, a PDI of from about 1.4 to about 5.0 (Mw/Mn), a Mz of from about 250 kDa to about 5,000 kDa, and a PDI pf from about 1.4 to about 15.0 (Mz/Mw).

In certain embodiments, during step (a), the raw dextran material is contacted with the oxidizing agent at a temperature of about 0° C., about 5° C., about 10° C., about 15° C., about 20° C., about 25° C., about 30° C., about 35° C., about 40° C., about 45° C., or about 50° C. In certain embodiments, in step (a), the raw dextran material is contacted with the oxidizing agent at a temperature from about 0° C. to about 50° C., from about 10° C. to about 50° C., from about 20° C. to about 50° C., from about 30° C. to about 50° C., from about 40° C. to about 50° C., from about 10° C. to about 40° C., from about 10° C. to about 30° C., from about 10° C. to about 20° C., from about 20° C. to about 40° C., from about 20° C. to about 30° C., or from about 30° C. to about 40° C. In certain embodiments, in step (a), the raw dextran material is contacted with the oxidizing agent at a temperature from about 0° C. to about 50° C.

In certain embodiments, during step (a), the oxidizing agent is a periodate salt. In certain embodiments, the periodate salt is selected from the group consisting of sodium periodate or potassium periodate.

In certain embodiments, during step (b), the oxidized dextran is purified using a method selected from the group consisting of dialysis, gel filtration chromatography, stirred cell filtration, tangential flow filtration, and combinations thereof.

In certain embodiments, during step (b), purification of the oxidized dextran intermediate removes greater than 70%, 75%, 80%, 85%, 90%, or 95% of oxidized dextran species with a molecular weight of less than 1.4 kDa. In certain embodiments, during step (b), the purification of the oxidized dextran intermediate removes greater than 90% of oxidized dextran species with a molecular weight of less than 1.4 kDa.

Without wishing to be bound by theory, it is contemplated that purification of the oxidized dextran intermediate to remove some or all of the low molecular weight oxidized dextran species (e.g., less than 1.4 kDa) increases the ratio of primary aldehyde groups to secondary aldehyde groups in the oxidized dextran composition. It is believed that increasing the number of primary aldehydes in the oxidized dextran composition facilitates a denser network of Schiff base linkages between oxidized dextran and acrylated chitosan than could be achieved without the purification step.

In certain embodiments, the yield of oxidized dextran obtained following step (b) is from about 60% to about 100%, from about 65% to about 100%, from about 70% to about 100%, from about 75% to about 100%, from about 80% to about 100%, from about 85% to about 100%, from about 90% to about 100%, from about 95% to about 100%, from about 60% to about 95%, from about 60% to about 90%, from about 60% to about 85%, from about 60% to about 80%, from about 60% to about 75%, from about 60% to about 70%, from about 60% to about 65%, from about 65% to about 95%, from about 65% to about 90%, from about 65% to about 85%, from about 65% to about 80%, from about 65% to about 75%, from about 65% to about 70%, from about 70% to about 95%, from about 70% to about 90%, from about 70% to about 85%, from about 70% to about 80%, from about 70% to about 75%, from about 75% to about 95%, from about 75% to about 90%, from about 75% to about 85%, from about 75% to about 80%, from about 80% to about 95%, from about 80% to about 90%, from about 80% to about 85%, from about 85% to about 95%, from about 85% to about 90%, or from about 90% to about 95%. In certain embodiments, the yield of oxidized dextran obtained following step (b) is from about 60% to about 95%.

In certain embodiments, the method further comprising the step of precipitating the oxidized dextran composition to provide a solid. In certain embodiments, the method further comprising the step of lyophilizing the oxidized dextran composition to provide a solid.

In certain embodiments, the method further comprising the step of dissolving the solid into an aqueous medium to form a solution comprising an amount of the oxidized dextran composition.

In certain embodiments, the amount of the oxidized dextran composition in the solution is about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, about 10%, about 11%, about 12%, about 13%, about 14%, about 15%, about 16%, about 17%, about 18%, about 19%, about 20%, about 21%, about 22%, about 23%, about 24%, or about 25% by weight of the total weight of the solution.

In certain embodiments, the amount of the oxidized dextran composition in the solution is from about 1% to about 25%, from about 1% to about 20%, from about 1% to about 15%, from about 1% to about 10%, from about 1% to about 9%, from about 1% to about 8%, from about 1% to about 7%, from about 1% to about 6%, from about 1% to about 5%, from about 1% to about 4%, from about 1% to about 3%, from about 1% to about 2%, from about 2% to about 10%, from about 2% to about 9%, from about 2% to about 8%, from about 2% to about 7%, from about 2% to about 6%, from about 2% to about 5%, from about 2% to about 4%, from about 2% to about 3%, from about 3% to about 10%, from about 3% to about 9%, from about 3% to about 8%, from about 3% to about 7%, from about 3% to about 6%, from about 3% to about 5%, from about 3% to about 4%, from about 4% to about 10%, from about 4% to about 9%, from about 4% to about 8%, from about 4% to about 7%, from about 4% to about 6%, from about 4% to about 5%, from about 5% to about 10%, from about 5% to about 9%, from about 5% to about 8%, from about 5% to about 7%, from about 5% to about 6%, from about 6% to about 10%, from about 6% to about 9%, from about 6% to about 8%, from about 6% to about 7%, from about 7% to about 10%, from about 7% to about 9%, from about 7% to about 8%, from about 8% to about 10%, from about 8% to about 9%, or from about 9% to about 10% by weight of the total weight of the solution.

In certain embodiments, the amount of the oxidized dextran composition in the solution is from about 1% (w/w) to about 25% (w/w) by weight of the total weight of the solution. In certain embodiments, the amount of the oxidized dextran composition in the solution is from about 1% (w/w) to about 10% (w/w) by weight of the total weight of the solution. In certain embodiments, the amount of the oxidized dextran composition in the solution is from about 2% (w/w) to about 5% (w/w), about 4% (w/w) to about 7% (w/w), or about 6% (w/w) to about 9% (w/w) by weight of the total weight of the solution.

In another aspect, provided herein is a method of preparing an oxidized dextran composition comprising:

-   -   (a) contacting a raw dextran material with a periodate salt to         form an oxidized dextran intermediate, wherein the raw dextran         material has a PDI of from about 1.4 to about 5.0; and     -   (b) purifying the oxidized dextran intermediate to produce an         oxidized dextran composition of the present invention.

In certain embodiments, the oxidized dextran composition produced in step (b) is the oxidized dextran composition described herein.

In certain embodiments, the periodate salt is selected from the group consisting of sodium periodate or potassium periodate.

In certain embodiments, the yield of oxidized dextran obtained following step (b) is from about 60% to about 95%.

In certain embodiments, the method further comprising the step of precipitating the oxidized dextran composition to provide a solid. In certain embodiments, the method further comprising the step of lyophilizing the oxidized dextran composition to provide a solid.

In certain embodiments, the amount of the oxidized dextran composition in the solution is from about 1% (w/w) to about 10% (w/w) by weight of the total weight of the solution.

The invention provides an oxidized dextran composition described herein produced by the methods described herein.

VI Methods of Making Hemostatic Hydrogel Compositions

The hemostatic hydrogels of the present invention represent a three-dimensional dynamic network that forms with reversible covalent bonds. The dynamic network is modulated by a variety of properties including, among other things, the properties of the two precursor compositions of the present invention, namely the acrylated chitosan and oxidized dextran compositions. Without wishing to be bound by theory, it is believed that the formation of the hydrogel composition is a two-step process. In the first step, the acrylated chitosan and oxidized dextran polymer chains intertwine, resulting in the formation of hydrogen bonding between the acrylated chitosan and oxidized dextran chains. In the second step, a Schiff base group forms between the aldehyde groups present in the oxidized dextran and the free amino group of the acrylated chitosan. The localized reaction between one monomer of the oxidized dextran (in its aldehyde form) and one monomer of the acrylated chitosan to link via Schiff base formation is depicted below:

Schiff base formation is a reversible reaction with equilibrium favoring formation of the Schiff base. This reversibility in Schiff base formation may impact the biodegradation of the hydrogel over time. It is contemplated more unreacted aldehydes on the oxidized dextran backbone come in contact with unreacted amines on the acrylated chitosan backbone to form additional Schiff base links as the hydrogel system seeks to achieve a lower energy structure. The polymer chains reorient into a more compact hydrogel with a reduced spatial volume that exudes water as it shrinks (see, FIGS. 6-8). The reversibility of Schiff base formation results in a dynamic and transient hydrogel network. The dynamics of the hydrogel network are thought to be influenced by the Mw and PDI of the acrylated chitosan and oxidized dextran compositions, the ratio of aldehyde and amine groups and salt concentration. It is believed that the dynamics of the hydrogel network may be controlled by modifying one or more of these parameters.

The kinetics of hydrogel formation are important for the function of the hydrogel as a hemostat given, among other things, the desire to rapidly stop blood loss or leakage in tissues of interest. It is believed that the hydrogel compositions of the present invention have three different reaction kinetics occurring concurrently. The initial reaction kinetics of gel formation are considered rapid enough for the hydrogel to adhere to tissue and gain enough cohesive strength and stiffness in a short period of time (e.g., from about 5 to about 30 seconds) to stem the blood flow. During this short period of time, the initial kinetics also forms a trabeculated, non-interconnected pore structure with a large pore size distribution (see, FIG. 1). These features contribute to the collection, retention and concentration of platelets and red blood cells (RBCs) within the pore structure of the hydrogel. The surface roughness of this pore structure facilitates platelet adhesion, activation and aggregation (e.g., soft clot or platelet plug) which are the first steps in activating the coagulation cascade (see, FIG. 2). Once the coagulation cascade is triggered, fibrin strands are formed through biochemical pathways. The fibrin strands trap more platelets and red blood cells, thereby forming a stable blood clot. The secondary rate kinetics of additional Schiff base formation appear to be slower and retain the concentrated platelets and RBCs locally to promote coagulation. The lack of swelling in the hydrogel avoids dilution of the platelets and RBCs, as might be observed in other matrices that expand (e.g., gelatin-based hemostats, cellulose based hemostats), and results in more effective aggregation and concentration that is required for coagulation. The third-rate kinetics relate to the rate of degradation of the hydrogel. This rate is fast enough to allow continuous shrinkage and eventual degradation within a physiologically relevant time frame over days, weeks and months.

The invention provides methods of preparing hemostatic hydrogel compositions. In various embodiments, the methods generally include contacting an acrylated chitosan composition disclosed herein with an oxidized dextran composition disclosed herein.

In certain embodiments, the ratio of the viscosity of the acrylated chitosan composition to the oxidized dextran composition ranges from about 50:1 to about 10,000:1, from about 100:1 to about 10,000:1, from about 500:1 to about 10,000:1, from about 1,000:1 to about 10,000:1, from about 5,000:1 to about 10,000:1, from about 50:1 to about 5,000:1, from about 50:1 to about 1,000:1, from about 50:1 to about 500:1, from about 50:1 to about 100:1, from about 100:1 to about 5,000:1, from about 100:1 to about 1,000:1, from about 100:1 to about 500:1, from about 500:1 to about 5,000:1, from about 500:1 to about 1,000:1, or from about 1,000:1 to about 5,000:1. In certain embodiments, the ratio of the viscosity of the acrylated chitosan composition to the oxidized dextran composition ranges from about 100:1 to about 10,000:1.

In certain embodiments, the ratio of the volume of acrylated chitosan solution to the volume of oxidized dextran solution is about 10:1, about 9:1, about 8:1, about 7:1, about 6:1, about 5:1, about 4:1, about 3:1, about 2:1, about 1:1, about 1:2, about 1:3, about 1:4, about 1:5, about 1:6, about 1:7, about 1:8, about 1:9, or about 1:10.

In certain embodiments, the resulting hemostatic hydrogel composition is a hemostatic hydrogel composition disclosed herein. However, it is appreciated that the hydrogel achieves its hemostatic properties and blood coagulation properties in the absence of an additional blood clotting agent that promotes blood clotting or otherwise activates the blood clotting cascade (e.g., Factor XIII, Factor IX, Factor X, Factor XI, Factor XII, or thrombin). As a result, in certain embodiments, the oxidized dextran, acrylated chitosan, and the hemostatic hydrogel produced by combining the acrylated chitosan and oxidized dextran are substantially free of one or more exogenously added blood clotting agents. In this context, the term “substantially free” of an exogenously added blood clotting agent is understood to mean an amount of the exogenously added agent that is less than is necessary to produce a blood clot in a standard blood clotting assay.

In certain embodiments, the hemostatic hydrogel composition further comprises a therapeutic agent. In certain embodiments, the therapeutic agent is selected from the group consisting of a small molecule drug, peptide (e.g., hormone), protein, for example, hormone, growth factor, and antibody. In certain embodiments, the small molecule drug compound is selected from the group comprising an antibiotic, a non-steroidal anti-inflammatory agent, an anti-cancer agent, an antimicrobial.

In certain embodiments, the therapeutic agent can include, without limitation, a polynucleotide (e.g., DNA, RNA), an oligonucleotide, a gene therapy agent, a nucleoside analog (e.g., Cytovene, Epivir, Gemzar, Hivid, Rebetron, Videx, Zerit, Zovirax), a polynucleic acid decoy, a peptide (e.g., peptide hormone), a protein (e.g., a therapeutic antibody, e.g., Ig A, Ig G, Ig M, Ig D, and Ig E antibodies), or a growth factor (e.g., bone morphic growth factor (BMP), angiopoietin, acidic fibroblast growth factor (aFGF), basic fibroblast growth factor (bFGF), vascular endothelial growth factor (vEGF), platelet derived growth factor (PDGF), nerve growth factor (NGF)), an anti-inflammatory drug (e.g., dexamethasone), an immune suppressive agent, an anti-neoplastic agent, an anti-cancer agent, an anti-cell proliferation agent, a nitric oxide releasing agent, an anti-diabetic drug (e.g., rosigliatazone), an antibiotic (e.g., Minocycline, Rifampin, Erythromycin, Novobiocin), an anti-microbial agent (e.g., Triclosan, Fusidic acid, Silver acetate, Polymyxin), an analgesic (e.g., codeine, meperidine, morphine, aspirin, acetaminophen, d-propoxyphene), a burn care agent (e.g., silver sulfadiazine, bacitracin, benzocaine) or any combination thereof. In certain embodiments, the therapeutic agent may be added to the acrylated chitosan composition and/or the oxidized dextran composition prior to contacting the acrylated chitosan composition with the oxidized dextran composition.

In certain embodiments, the hemostatic hydrogel composition further comprises a plurality of cells, for example, immune cells (for example, genetically modified immune cells such as genetically modified B-cells or T-cells, such as CART cells) and stem cells. In certain embodiments, the stem cells are selected from the group comprising mesenchymal stem cells, pancreatic stem cells, pluripotent stem cells, neural stem cells, hematopoietic stem cells or any combination thereof. The cells may be added to the acrylated chitosan composition and/or the oxidized dextran composition prior to contacting the acrylated chitosan composition with the oxidized dextran composition.

In certain embodiments, the acrylated chitosan composition is contacted with the oxidized dextran composition in a static mixer, and optionally or in addition the mixture is aerosolized prior to application to tissue. In certain embodiments, the mixture is aerosolized using an air-assisted spray tip or an unassisted spray tip.

In certain embodiments, the gelation time of the hemostatic hydrogel composition ranges within from about 1 second to about 300 seconds, from about 1 second to about 240 seconds, from about 1 second to about 180 seconds, from about 1 second to about 120 seconds, from about 1 second to about 60 seconds, from about 1 second to about 30 seconds, from about 1 second to about 25 seconds, from about 1 second to about 20 seconds, from about 1 second to about 15 seconds, from about 1 second to about 10 seconds, from about 1 second to about 5 seconds, from about 5 seconds to about 300 seconds, from about 5 seconds to about 240 seconds, from about 5 seconds to about 180 seconds, from about 5 seconds to about 120 seconds, from about 5 seconds to about 60 seconds, from about 5 seconds to about 30 seconds, from about 5 seconds to about 25 seconds, from about 5 seconds to about 20 seconds, from about 5 seconds to about 15 seconds, from about 5 seconds to about 10 seconds, from about 7 seconds to about 300 seconds, from about 7 seconds to about 240 seconds, from about 7 seconds to about 180 seconds, from about 7 seconds to about 120 seconds, from about 7 seconds to about 60 seconds, from about 7 seconds to about 30 seconds, from about 7 seconds to about 25 seconds, from about 7 seconds to about 20 seconds, from about 7 seconds to about 15 seconds, from about 7 seconds to about 10 seconds, from about 10 seconds to about 300 seconds, from about 10 seconds to about 240 seconds, from about 10 seconds to about 180 seconds, from about 10 seconds to about 120 seconds, from about 10 seconds to about 60 seconds, from about 10 seconds to about 30 seconds, from about 10 seconds to about 25 seconds, from about 10 seconds to about 20 seconds, from about 10 seconds to about 15 seconds, or from about from about 20 seconds to about 30 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition.

In certain embodiments, the gelation time of the hemostatic hydrogel composition is less than 5 seconds, less than 10 seconds, less than 15 seconds, less than 20 seconds, less than 30 seconds, less than 60 seconds, less than 120 seconds, less than 180 seconds, less than 240 seconds, or less than 300 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition. In certain embodiments, the gelation time of the hemostatic hydrogel composition is less than 30 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition.

In certain embodiments, the gelation time of the hemostatic hydrogel composition is within from 1 second to 30 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition. In certain embodiments, the gelation time of the hemostatic hydrogel composition is within 5 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition. In certain embodiments, the gelation time of the hemostatic hydrogel composition is within 10 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition. In certain embodiments, the gelation time of the hemostatic hydrogel composition is within 15 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition. In certain embodiments, the gelation time of the hemostatic hydrogel composition is within 20 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition. In certain embodiments, the gelation time of the hemostatic hydrogel composition is within 25 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition. It is contemplated that the hemostatic hydrogel compositions of the present invention that have a gelation time of within 25, 20, 15, or 10 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition may be useful in the treatment of wounds resulting from certain minimally invasive surgeries.

In certain embodiments, the gelation time of the hemostatic hydrogel composition is within from about 10 seconds to about 240 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition. In certain embodiments, the gelation time of the hemostatic hydrogel composition is within about 10 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition. In certain embodiments, the gelation time of the hemostatic hydrogel composition is within about 240 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition. Depending upon the circumstances, it is contemplated that hemostatic hydrogel compositions of the present invention having a gelation time of within 240 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition may be useful in the treatment of wounds resulting from certain minimally invasive surgeries.

VII Properties of Hemostatic Hydrogel Compositions

The hemostatic hydrogels described herein have a variety of structural and/or structural/functional features.

(i) Structural Features

For example, the hemostatic hydrogel compositions comprise two or more of the following features, which include (i) a total amount of free aldehyde groups of from about 0.1 to about 0.7 moles aldehyde/mole oxidized dextran, (ii) the hemostatic hydrogel composition is formed from oxidized dextran and acrylated chitosan, wherein the ratio of primary aldehydes in the oxidized dextran to the amines in the acrylated chitosan is in the range from about 1.0 to about 2.0, and/or the ratio of total aldehydes in the oxidized dextran to amines in the acrylated chitosan is from about 1.5 to about 3.0, (iii) the ratio of Mw of the acrylated chitosan to the oxidized dextran is from about 2 to about 10, the ratio of Mn of the acrylated chitosan to the oxidized dextran is from about 4 to about 15, the ratio of Mz of the acrylated chitosan to the oxidized dextran is from about 2 to about 10, the ratio of PDI (Mw/Mn) of acrylated chitosan to oxidized dextran is from about 0.5 to about 0.8, and/or the ratio of PDI (Mz/Mw) of acrylated chitosan to oxidized dextran is from about 0.5 to about 1.0, (iv) upon formation of the hemostatic hydrogel composition, the hemostatic hydrogel composition comprises a bound water content of from about 65% w/w to about 95% w/w, (v) a three-dimensional porous structure comprising layers of substantially non-interconnected pores having (a) a pore size distribution from about 10 μm to about 850 μm in diameter, (b) a platelet adhesive surface, or a combination of (a) and (b), and/or (vi) the hemostatic hydrogel composition comprises walls disposed between the substantially non-interconnected pores, the walls having a wall thickness of from 0.046 μm to 50 μm.

In certain embodiments, the hemostatic hydrogel composition increases in burst strength over time. For example, in certain embodiments (i) at about 10 seconds after the formation of the hemostatic hydrogel composition, the hemostatic hydrogel composition has a burst strength of greater than 20 mmHg as determined using an ASTM F 2392-04 protocol, (ii) at about 2 minutes after the formation of the hemostatic hydrogel composition, the hemostatic hydrogel composition has a burst strength of greater than about 35 mmHg as determined using an ASTM F 2392-04 protocol, and/or (iii) at about 5 minutes after the formation of the hemostatic hydrogel composition, the hemostatic hydrogel composition has a burst strength of greater than about 70 mmHg as determined using an ASTM F 2392-04 protocol. In certain embodiments, the hemostatic hydrogel composition (i) has an elastic modulus of from about 500 Pa to about 5000 Pa at from about 10 seconds to about 80 seconds after the formation of the hemostatic hydrogel composition, (ii) has a compression modulus of from about 3 kPa to about 250 kPa, and/or (iii) has an average adhesion strength of from about 1.0 N to about 50.0 N, as determined using an ASTM F 2258-05 protocol.

In certain embodiments, the volume of the hemostatic hydrogel composition (i) when formed, does not swell upon exposure to a physiological fluid or body fluid, (ii) shrinks by less than about 5%, for example, less than about 5%, 3%, 2% about 10 minutes after formation when exposed to a physiological fluid or body fluid and/or (iii) shrinks from about 5% to about 30% within about 2 hours after formation, from about 20% to about 60% within about 8 hours after formation, and from about 45% to about 70% within about 24 hours after formation, when exposed to a temperature of 37° C. and 75% relative humidity.

In certain embodiments, the hemostatic hydrogel composition is substantially transparent when the hemostatic hydrogel composition has a thickness of 2 mm to 10 mm. This permits a medical practitioner (e.g., surgeon) to visualize the underlying tissue and/or tissue lesion after application of the hemostat to confirm that bleeding has slowed or stopped.

In certain embodiments, the hemostatic hydrogel composition comprises a total amount of free aldehyde groups of from about 0.1 to about 0.7, from about 0.1 to about 0.6, from about 0.2 to about 0.6, from about 0.3 to about 0.6, from about 0.4 to about 0.6, from about 0.5 to about 0.6, from about 0.1 to about 0.5, from about 0.1 to about 0.4, from about 0.1 to about 0.3, from about 0.1 to about 0.2, from about 0.2 to about 0.5, from about 0.2 to about 0.4, from about 0.2 to about 0.3, from about 0.3 to about 0.5, from about 0.3 to about 0.4, or from about 0.4 to about 0.5 moles aldehyde/mole oxidized dextran. In certain embodiments, the hemostatic hydrogel composition comprises a total amount of free aldehyde groups of from about 0.1 to about 0.7 moles aldehyde/mole oxidized dextran. In certain embodiments, the hemostatic hydrogel composition comprises a total amount of free aldehyde groups of from about 0.2 to about 0.5 moles aldehyde/mole oxidized dextran.

In certain embodiments, the ratio of primary aldehydes in the oxidized dextran to the amines in the acrylated chitosan is in the range from about 1.0 to about 2.0, from about 1.2 to about 2.0, from about 1.4 to about 2.0, from about 1.6 to about 2.0, from about 1.8 to about 2.0, from about 1.0 to about 1.2, from about 1.0 to about 1.4, from about 1.0 to about 1.6, from about 1.0 to about 1.8, from about 1.2 to about 1.4, from about 1.2 to about 1.6, from about 1.2 to about 1.8, from about 1.4 to about 1.6, from about 1.4 to about 1.8, or from about 1.6 to about 1.8. In certain embodiments, the ratio of primary aldehydes in the oxidized dextran to the amines in the acrylated chitosan is in the range from about 1.0 to about 1.8.

In certain embodiments, the ratio of total aldehydes in the oxidized dextran to amines in the acrylated chitosan is from about 1.5 to about 3.0, from about 2.0 to about 3.0, from about 2.5 to about 3.0, from about 1.5 to about 2.5, from about 1.5 to about 2.0, or from about 2.0 to about 2.5. In certain embodiments, the ratio of total aldehydes in the oxidized dextran to amines in the acrylated chitosan is from about 1.5 to about 2.8.

In certain embodiments, the ratio of Mw of the acrylated chitosan to the oxidized dextran is from about 2 to about 10, from about 4 to about 10, from about 6 to about 10, from about 8 to about 10, from about 2 to about 8, from about 2 to about 6, from about 2 to about 4, from about 4 to about 8, from about 4 to about 6, or about from about 6 to about 8. In certain embodiments, the ratio of Mw of the acrylated chitosan to the oxidized dextran is from about 4 to about 8.

In certain embodiments, the ratio of Mn of the acrylated chitosan to the oxidized dextran is from about 4 to about 15, from about 8 to about 15, from about 12 to about 15, from about 4 to about 12, from about 4 to about 8, or from about 8 to about 12. In certain embodiments, the ratio of Mn of the acrylated chitosan to the oxidized dextran is from about 8 to about 15.

In certain embodiments, the ratio of Mz of the acrylated chitosan to the oxidized dextran is from about 2 to about 10, from about 4 to about 10, from about 6 to about 10, from about 8 to about 10, from about 2 to about 8, from about 2 to about 6, from about 2 to about 4, from about 4 to about 8, from about 4 to about 6, or from about 6 to about 8. In certain embodiments, the ratio of Mz of the acrylated chitosan to the oxidized dextran is from about 4 to about 8.

In certain embodiments, the ratio of PDI (Mw/Mn) of acrylated chitosan to oxidized dextran is from about 0.5 to about 0.8, from about 0.6 to about 0.8, from about 0.7 to about 0.8, from about 0.5 to about 0.7, from about 0.5 to about 0.6, or from about 0.6 to about 0.7. In certain embodiments, the ratio of PDI (Mw/Mn) of acrylated chitosan to oxidized dextran is from about 0.5 to about 0.7.

In certain embodiments, the ratio of PDI (Mz/Mw) of acrylated chitosan to oxidized dextran is from about 0.5 to about 1.0, from about 0.6 to about 1.0, from about 0.7 to about 1.0, from about 0.8 to about 1.0, from about 0.9 to about 1.0, from about 0.5 to about 0.9, from about 0.5 to about 0.8, from about 0.5 to about 0.7, from about 0.5 to about 0.6, from about 0.6 to about 0.9, from about 0.6 to about 0.8, from about 0.6 to about 0.7, from about 0.7 to about 0.9, from about 0.7 to about 0.8, or from about 0.8 to about 0.9. In certain embodiments, the ratio of PDI (Mz/Mw) of acrylated chitosan to oxidized dextran is from about 0.8 to about 1.0.

In certain embodiments, upon formation of the hemostatic hydrogel composition, the hemostatic hydrogel composition comprises a bound water content of from about 60% (w/w) to about 99% (w/w), from about 65% (w/w) to about 99% (w/w), from about 70% (w/w) to about 99% (w/w), from about 75% (w/w) to about 99% (w/w), from about 80% (w/w) to about 99% (w/w), from about 85% (w/w) to about 99% (w/w), from about 90% (w/w) to about 99% (w/w), from about 95% (w/w) to about 99% (w/w), from about 60% (w/w) to about 95% (w/w), from about 60% (w/w) to about 90% (w/w), from about 60% (w/w) to about 85% (w/w), from about 60% (w/w) to about 80% (w/w), from about 60% (w/w) to about 75% (w/w), from about 60% (w/w) to about 70% (w/w), from about 60% (w/w) to about 65% (w/w), from about 65% (w/w) to about 95% (w/w), from about 65% (w/w) to about 90% (w/w), from about 65% (w/w) to about 85% (w/w), from about 65% (w/w) to about 80% (w/w), from about 65% (w/w) to about 75% (w/w), from about 65% (w/w) to about 70% (w/w), from about 70% (w/w) to about 95% (w/w), from about 70% (w/w) to about 90% (w/w), from about 70% (w/w) to about 85% (w/w), from about 70% (w/w) to about 80% (w/w), from about 70% (w/w) to about 75% (w/w), from about 75% (w/w) to about 95% (w/w), from about 75% (w/w) to about 90% (w/w), from about 75% (w/w) to about 85% (w/w), from about 75% (w/w) to about 80% (w/w), from about 80% (w/w) to about 95% (w/w), from about 80% (w/w) to about 90% (w/w), from about 80% (w/w) to about 85% (w/w), from about 85% (w/w) to about 95% (w/w), from about 85% (w/w) to about 90% (w/w), or from about 90% (w/w) to about 95% (w/w). In certain embodiments, upon formation of the hemostatic hydrogel composition, the hemostatic hydrogel composition comprises a bound water content of from about 65% (w/w) to about 95% (w/w).

In certain embodiments, the hemostatic hydrogel composition comprises a three-dimensional porous structure, that comprises layers of substantially non-interconnected pores (see, e.g., FIG. 1). In certain embodiments, the layers of substantially non-interconnected pores comprise anisotropic pores and/or isotropic pores. In certain embodiments, the layers of substantially non-interconnected pores comprise both anisotropic pores and isotropic pores. In certain embodiments, the pores have a pore size distribution from about 10 μm to about 850 μm in diameter, where the diameter of a pore is the longest possible straight-line distance between the edges of the pore.

In certain embodiments, the ratio of the pore volume to the hydrogel volume is from about 0.9 to about 0.98. In certain embodiments, the ratio of the volume of the walls disposed between the pores to the hydrogel volume is from about 0.02 to about 0.09. In certain embodiments, the ratio of the pore volume to the volume of the walls disposed between the pores is from about 10 to about 33.

In certain embodiments, at about 2 minutes after the formation of the hemostatic hydrogel composition, the hemostatic hydrogel composition has a burst strength of from about 35 mmHg to about 80 mmHg, from about 40 mmHg to about 80 mmHg, from about 45 mmHg to about 80 mmHg, from about 50 mmHg to about 80 mmHg, from about 60 mmHg to about 80 mmHg, from about 70 mmHg to about 80 mmHg, from about 35 mmHg to about 70 mmHg, from about 35 mmHg to about 60 mmHg, from about 35 mmHg to about 50 mmHg, from about 35 mmHg to about 45 mmHg, from about 35 mmHg to about 40 mmHg, from about 40 mmHg to about 80 mmHg, from about 40 mmHg to about 70 mmHg, from about 40 mmHg to about 60 mmHg, from about 40 mmHg to about 50 mmHg, from about 40 mmHg to about 45 mmHg, from about 50 mmHg to about 80 mmHg, from about 50 mmHg to about 70 mmHg, from about 50 mmHg to about 60 mmHg, from about 60 mmHg to about 80 mmHg, or from about 60 mmHg to about 70 mmHg, as determined using an ASTM F 2392-04 protocol.

In certain embodiments, at about 5 minutes after the formation of the hemostatic hydrogel composition, the hemostatic hydrogel composition has a burst strength of from about 50 mmHg to about 125 mmHg, from about 60 mmHg to about 125 mmHg, from about 70 mmHg to about 125 mmHg, from about 80 mmHg to about 125 mmHg, from about 90 mmHg to about 125 mmHg, from about 100 mmHg to about 125 mmHg, from about 50 mmHg to about 100 mmHg, from about 50 mmHg to about 90 mmHg, from about 50 mmHg to about 85 mmHg, from about 50 mmHg to about 80 mmHg, from about 50 mmHg to about 75 mmHg, from about 50 mmHg to about 70 mmHg, from about 50 mmHg to about 60 mmHg, from about 60 mmHg to about 100 mmHg, from about 60 mmHg to about 90 mmHg, from about 60 mmHg to about 85 mmHg, from about 60 mmHg to about 80 mmHg, from about 60 mmHg to about 75 mmHg, from about 60 mmHg to about 70 mmHg, from about 70 mmHg to about 115 mmHg, from about 70 mmHg to about 110 mmHg, from about 70 mmHg to about 100 mmHg, from about 70 mmHg to about 90 mmHg, from about 70 mmHg to about 85 mmHg, from about 70 mmHg to about 80 mmHg, from about 70 mmHg to about 75 mmHg, from about 75 mmHg to about 110 mmHg, from about 75 mmHg to about 100 mmHg, from about 75 mmHg to about 90 mmHg, from about 75 mmHg to about 85 mmHg, from about 75 mmHg to about 80 mmHg, from about 80 mmHg to about 110 mmHg, from about 80 mmHg to about 100 mmHg, from about 80 mmHg to about 90 mmHg, from about 85 mmHg to about 110 mmHg, from about 85 mmHg to about 100 mmHg, from about 85 mmHg to about 90 mmHg, from about 80 mmHg to about 85 mmHg, from about 90 mmHg to about 110 mmHg, from about 90 mmHg to about 100 mmHg, or from about 100 mmHg to about 110 mmHg, as determined using an ASTM F 2392-04 protocol.

In certain embodiments, at about 5 minutes after the formation of the hemostatic hydrogel composition, the hemostatic hydrogel composition has a burst strength of about 50 mmHg, about 55 mmHg, about 60 mmHg, about 65 mmHg, about 70 mmHg, about 75 mmHg, about 80 mmHg, about 85 mmHg, about 90 mmHg, about 95 mmHg, about 100 mmHg, about 105 mmHg, about 110 mmHg, about 115 mmHg, about 120 mmHg, or about 125 mmHg, as determined using an ASTM F 2392-04 protocol.

In certain embodiments, the hemostatic hydrogel composition, when formed, does not swell upon exposure to a physiological fluid or body fluid.

In certain embodiments, the volume of the hemostatic hydrogel composition shrinks by less than about 1.0%, about 1.2%, about 1.4%, about 1.6%, about 1.8%, about 2.0%, about 2.2%, about 2.4%, about 2.6%, about 2.8%, about 3.0%, about 3.2%, about 3.4%, about 3.6%, about 3.8%, about 4.0%, about 4.2%, about 4.4%, about 4.6%, about 4.8%, or about 5%, within about 10 minutes after formation when exposed to a physiological fluid or body fluid.

In certain embodiments, the hemostatic hydrogel composition shrinks from about 1% to about 40%, from about 5% to about 40%, from about 10% to about 40%, from about 20% to about 40%, from about 30% to about 40%, from about 1% to about 30%, from about 1% to about 20%, from about 1% to about 10%, from about 1% to about 5%, from about 5% to about 30%, from about 5% to about 20%, from about 5% to about 10%, from about 10% to about 30%, from about 10% to about 20%, or from about 20% to about 30% within about 2 hours after formation, when exposed to a temperature of 37° C. and 75% relative humidity.

In certain embodiments, the hemostatic hydrogel composition shrinks from about 15% to about 65%, from about 20% to about 65%, from about 30% to about 65%, from about 40% to about 65%, from about 50% to about 65%, from about 60% to about 65%, from about 15% to about 60%, from about 15% to about 50%, from about 15% to about 40%, from about 15% to about 30%, from about 15% to about 20%, from about 20% to about 60%, from about 20% to about 50%, from about 20% to about 40%, from about 20% to about 30%, from about 30% to about 60%, from about 30% to about 50%, about 30% to about 40%, from about 40% to about 60%, from about 40% to about 50%, or from about 50% to about 60%, within about 8 hours after formation, when exposed to a temperature of 37° C. and 75% relative humidity.

In certain embodiments, the hemostatic hydrogel composition shrinks from about 40% to about 75%, from about 45% to about 75%, from about 50% to about 75%, from about 55% to about 75%, from about 60% to about 75%, from about 65% to about 75%, from about 70% to about 75%, from about 40% to about 70%, from about 40% to about 65%, from about 40% to about 60%, from about 40% to about 55%, from about 40% to about 50%, from about 40% to about 45%, from about 45% to about 70%, from about 45% to about 65%, from about 45% to about 60%, from about 45% to about 55%, from about 45% to about 50%, from about 50% to about 70%, from about 50% to about 65%, from about 50% to about 60%, from about 50% to about 55%, from about 55% to about 70%, from about 55% to about 65%, from about 55% to about 60%, from about 60% to about 70%, from about 60% to about 65%, or from about 65% to about 70%, within about 24 hours after formation, when exposed to a temperature of 37° C. and 75% relative humidity.

In certain embodiments, the hemostatic hydrogel composition shrinks from about 5% to about 30% within about 2 hours after formation, from about 20% to about 60% within about 8 hours after formation, and from about 45% to about 70% within about 24 hours after formation, when exposed to a temperature of 37° C. and 75% relative humidity.

In certain embodiments, the hemostatic hydrogel composition shrinks from about 55% to about 75% within about 60 days after formation, when immersed in saline solution (e.g., blood bank saline solution (0.85% (w/v) NaCl) at about 25° C.

In certain embodiments, the hemostatic hydrogel composition is substantially transparent when the hemostatic hydrogel composition has a thickness of 2 mm to 10 mm. In certain embodiments, a substantially transparent hemostatic hydrogel composition maybe defined as any hemostatic hydrogel composition with a visible light % transmittance of greater than 65%, wherein the % transmittance of the hemostatic hydrogel composition is measured using a UV-vis spectrometer.

In certain embodiments, the hemostatic hydrogel comprises pores certain of which having platelet adhesive surfaces that are sufficiently rough to permit activated platelets and/or red blood cells to adhere to the platelet adhesive surfaces.

In certain embodiments, the hemostatic hydrogel compositions of the present invention comprise:

(a) from about 0.0 to about 0.3 mole fraction of a first monomer of formula (I)

(b) from about 0.02 to about 0.7 mole fraction of a second monomer of formula (III),

and

(c) about 0.0 to about 0.8 mole fraction of a third monomer of formula (V),

In certain embodiments, the hemostatic hydrogel composition comprises from about 0.0 to about 0.26, from about 0.05 to about 0.26, from about 0.1 to about 0.26, from about 0.15 to about 0.26, from about 0.2 to about 0.26, from about 0.0 to about 0.2, from about 0.0 to about 0.15, from about 0.0 to about 0.1, from about 0.0 to about 0.05, from about 0.05 to about 0.2, from about 0.05 to about 0.15, from about 0.05 to about 0.1, from about 0.1 to about 0.2, from about 0.1 to about 0.15, or from about 0.15 to about 0.2, mole fraction of the first monomer of formula (I). In certain embodiments, the hemostatic hydrogel composition comprises from about 0.0 to about 0.26 mole fraction of the first monomer of formula (I).

In certain embodiments, the hemostatic hydrogel composition comprises from about 0.03 to about 0.7, from about 0.03 to about 0.6, from about 0.05 to about 0.6, from about 0.1 to about 0.6, from about 0.3 to about 0.6, from about 0.5 to about 0.6, from about 0.03 to about 0.5, from about 0.03 to about 0.3, from about 0.03 to about 0.1, from about 0.03 to about 0.05, from about 0.05 to about 0.5, from about 0.05 to about 0.3, from about 0.05 to about 0.1, from about 0.1 to about 0.5, from about 0.1 to about 0.3, or from about 0.3 to about 0.5, mole fraction of the second monomer of formula (III). In certain embodiments, wherein the hemostatic hydrogel composition from about 0.03 to about 0.6 mole fraction of the second monomer of formula (III).

In certain embodiments, the hemostatic hydrogel composition comprises from about 0.02 to about 0.8, from about 0.04 to about 0.8, from about 0.0 to about 0.7, from about 0.02 to about 0.7, from about 0.04 to about 0.7, from about 0.1 to about 0.7, from about 0.3 to about 0.7, from about 0.5 to about 0.7, from about 0.04 to about 0.5, from about 0.04 to about 0.3, from about 0.04 to about 0.1, from about 0.1 to about 0.5, from about 0.1 to about 0.3, or from about 0.3 to about 0.5, mole fraction of the third monomer of formula (V). In certain embodiments, the hemostatic hydrogel composition comprises from about 0.04 to about 0.7 mole fraction of the third monomer of formula (V).

In certain embodiments, wherein the hemostatic hydrogel composition comprises no greater than about 0.2 mole fraction of a fourth monomer of formula (IV)

In certain embodiments, the hemostatic hydrogel composition further comprises from about 0.0 to about 0.2, from about 0.05 to about 0.2, from about 0.1 to about 0.2, from about 0.15 to about 0.2, from about 0.0 to about 0.15, from about 0.0 to about 0.1, from about 0.0 to about 0.05, from about 0.05 to about 0.15, from about 0.05 to about 0.1, or from about 0.1 to about 0.15, mole fraction of the fourth monomer of formula (IV).

In certain embodiments, the hemostatic hydrogel composition comprises no greater than about 0.65 mole fraction of a fifth monomer of formula (VIII)

In certain embodiments, the hemostatic hydrogel composition comprises from about 0.0 to about 0.65, from about 0.2 to about 0.65, from about 0.4 to about 0.65, from about 0.0 to about 0.4, from about 0.0 to about 0.2, or from about 0.2 to about 0.4, mole fraction of a fifth monomer of formula (VIII).

In certain embodiments, the hemostatic hydrogel composition comprises a plurality of crosslinked moieties of formula (IX)

(ii) Structural/Functional Features

In certain embodiments, the hydrogels contain pores, certain of which have a platelet adhesive surface so that, when in contact with blood, the hemostatic hydrogel composition permits (i) platelets and/or red blood cells to bind to the platelet adhesive surface and promote blood clot formation at or within the hemostatic hydrogel composition, and/or (ii) platelets and/or red blood cells to adhere to the platelet adhesive surface and not permit platelets and/or red blood cells from the blood to enter pores present in a first surface of the hemostatic hydrogel composition, pass through the hemostatic hydrogel composition, and then exit the hemostatic hydrogel composition via pores present in a second surface of the hemostatic hydrogel composition that opposes the first surface.

The invention provides methods of promoting hemostasis (e.g., reducing or stopping blood loss) at a location in a subject in need thereof by applying a hemostatic hydrogel composition of the invention to the location to be treated in the subject.

In certain embodiments, the hemostatic hydrogel composition adheres to a tissue surface at the location. In certain embodiments, the hemostatic hydrogel composition adheres to the tissue surface at the location with average adhesion strength of from about 1.0 N to about 50.0 N, as determined using an ASTM F 2258-05 protocol.

In certain embodiments, platelets and/or red blood cells present at the location adhere to surfaces of pores in the hemostatic hydrogel composition.

In certain embodiments, the hemostatic hydrogel composition promotes platelet adhesion, platelet activation, and platelet aggregation at the site in need of hemostasis. During use, the hemostatic hydrogel composition promotes a blood coagulation cascade and blood clot formation at the site.

In certain embodiments, blood coagulation is achieved from about 10 seconds to about 300 seconds, from about 20 seconds to about 300 seconds, from about 30 seconds to about 300 seconds, from about 60 seconds to about 300 seconds, from about 120 seconds to about 300 seconds, from about 180 seconds to about 300 seconds, from about 240 seconds to about 300 seconds, from about 10 seconds to about 240 seconds, from about 10 seconds to about 180 seconds, from about 10 seconds to about 120 seconds, from about 10 seconds to about 60 seconds, from about 10 seconds to about 30 seconds, from about 10 seconds to about 20 seconds, from about 20 seconds to about 240 seconds, from about 20 seconds to about 180 seconds, from about 20 seconds to about 120 seconds, from about 20 seconds to about 60 seconds, from about 20 seconds to about 30 seconds, from about 30 seconds to about 240 seconds, from about 30 seconds to about 180 seconds, from about 30 seconds to about 120 seconds, from about 30 seconds to about 60 seconds, from about 60 seconds to about 240 seconds, from about 60 seconds to about 180 seconds, from about 60 seconds to about 120 seconds, from about 120 seconds to about 240 seconds, from about 120 seconds to about 180 seconds, or from about 180 seconds to about 240 seconds. In certain embodiments, when a hemostatic hydrogel composition of the present invention is applied to an abrasion, blood coagulation is achieved from about 20 seconds to about 210 seconds.

In certain embodiments, the hemostatic hydrogel compositions degrade within days, weeks (e.g., in 1 week, 2 weeks, 3 weeks, or 4 weeks) or months (e.g., two, three, four, five or six months).

In certain embodiments, the hemostatic hydrogel compositions of the present invention are biodegradable. Without wishing to be bound by theory it is believed that degradation of the hydrogels occurs by hydrolysis and enzymatic degradation. The degradation pathway may occur through a combination of two mechanisms. A first mechanism may involve cleavage of the crosslinks (e.g., the Schiff base linkages) between the polymer chains producing water soluble fragments. It is believed that the Schiff base linkages are reversible which leads to a progressive reorganization during which the polymer chains become degraded. A second mechanism may involve the degradation of the acrylated chitosan and oxidized dextran chains to produce smaller fragments (e.g., oligomers or monomers that are water soluble). Given that the hydrogel is formed from naturally occurring sugars, the products of degradation are non-toxic and are further degraded by the carbohydrate metabolism pathways or rapidly eliminated by the renal system.

It is believed that one of the rate limiting steps for the degradation process is the degree of acetylation (DA) of the acrylated chitosan. Given that certain enzymes, e.g., lysozyme, require a linear series of at least three N-acetylglucosamine units to cleave a glycidic link. Many enzymes have a hydrophobic pocket that interact with the polymer, e.g., around three linear N-acetylglucosamine subunits, and catalyzes the chain cleavage. The probability of having three N-acetylglucosamine units in a row is given by DA×DA×DA=DA³. As a result, as DA decreases, the probability of having three linear, adjacent N-acetylglucosamine subunits together drops as the third power DA. It is understood, however, that the rate of degradation can be modified or adjusted by altering the DA content of acrylated chitosan used to create the hydrogel.

In another aspect, provided is a hemostatic hydrogel composition comprising two or more of the following features:

-   -   (i) the hemostatic hydrogel composition comprises a         three-dimensional porous structure comprising layers of         substantially non-interconnected pores having (a) a pore size         distribution from about 10 μm to about 850 μm in diameter, (b) a         platelet adhesive surface, or a combination of (a) and (b),     -   (ii) the hemostatic hydrogel composition comprises walls         disposed between the substantially non-interconnected pores, the         walls having a wall thickness of from 0.046 μm to 50 μm,     -   (iii) the hemostatic hydrogel composition comprises a platelet         adhesive surface so that, when in contact with blood, the         hemostatic hydrogel composition permits platelets and/or red         blood cells within the blood to adhere to platelet adhesive         surface and promote blood clot formation at or within the         hemostatic hydrogel composition,     -   (iv) the hemostatic hydrogel composition comprises a platelet         adhesive surface so that, when in contact with blood, the         hemostatic hydrogel composition permits platelet and/or red         blood cells within the blood to adhere to the platelet adhesive         surface and not permit platelets and/or red blood cells from the         blood to enter pores present in a first surface of the         hemostatic hydrogel composition, pass through the hemostatic         hydrogel composition, and then exit the hemostatic hydrogel         composition via pores present in a second surface of the         hemostatic hydrogel composition that opposes the first surface,     -   (v) at about 10 seconds after the formation of the hemostatic         hydrogel composition, the hemostatic hydrogel composition has a         burst strength of greater than 20 mmHg as determined using an         ASTM F 2392-04 protocol,     -   (vi) at about 2 minutes after the formation of the hemostatic         hydrogel composition, the hemostatic hydrogel composition has a         burst strength of greater than about 35 mmHg as determined using         an ASTM F 2392-04 protocol,     -   (vii) at about 5 minutes after the formation of the hemostatic         hydrogel composition, the hemostatic hydrogel composition has a         burst strength of greater than about 70 mmHg as determined using         an ASTM F 2392-04 protocol,     -   (viii) the hemostatic hydrogel composition has an elastic         modulus of from about 500 Pa to about 5000 Pa at from about 10         seconds to about 80 seconds after the formation of the         hemostatic hydrogel composition,     -   (ix) the hemostatic hydrogel composition has a compression         modulus of from about 3 kPa to about 250 kPa,     -   (x) the hemostatic hydrogel composition has an average adhesion         strength of from about 1.0 N to about 50.0 N, as determined         using an ASTM F 2258-05 protocol,     -   (xi) the volume of the hemostatic hydrogel composition, when         formed, does not increase upon exposure to a physiological fluid         or body fluid,     -   (xii) the volume of the hemostatic hydrogel composition shrinks         by less than about 5% about 10 minutes after formation when         exposed to a physiological fluid or body fluid,     -   (xiii) the hemostatic hydrogel composition shrinks from about 5%         to about 30% about 2 hours after formation, from about 20% to         about 60% about 8 hours after formation, and/or from about 45%         to about 70% about 8 hours after formation, when exposed to a         temperature of 37° C. and 75% relative humidity,     -   (xiv) the hemostatic hydrogel composition is substantially         transparent when the hemostatic hydrogel composition has a         thickness of 2 mm to 10 mm, and     -   (xv) the hemostatic hydrogel composition optionally further         comprises a therapeutic agent.

In certain embodiments, the hydrogel comprises a gel produced by combining oxidized dextran with an acrylated chitosan composition produced by dissolving chitosan in an organic acid prior to acrylation. Examples of organic acids include, but are not limited to, acetic acid, citric acid, formic acid, lactic acid, malic acid, oxalic acid, and uric acid. In certain embodiments, the organic acid is acetic acid.

In another aspect, provided herein is a hemostatic hydrogel composition comprising a gel produced by combining oxidized dextran with acrylated chitosan, wherein the hemostatic hydrogel composition comprises a plurality of crosslinked moieties of formula (IX)

and further comprises one or more of the following features:

-   -   (i) the hemostatic hydrogel, when immersed in saline for about 4         hours exhibits a mass reduction of from about 1% to about 5%,     -   (ii) the hemostatic hydrogel, when immersed in saline for about         8 hours exhibits a mass reduction of from about 6% to about 10%,     -   (iii) the hemostatic hydrogel, when immersed in saline for about         24 hours exhibits a mass reduction of from about 20% to about         25%,     -   (iv) the hemostatic hydrogel, when exposed to a physiological         fluid or body fluid for about 8 hours exhibits an irreversible         decrease in volume, and     -   (v) the hemostatic hydrogel, at least 30 seconds after         formation, takes at least 5 minutes to completely dissolve when         exposed to a 5M hydroxylamine hydrochloride solution.

In certain embodiments, the hemostatic hydrogel, when immersed in saline for about 4 hours exhibits a mass reduction of from about 1% to about 5%, from about 2% to about 5%, from about 3% to about 5%, from about 4% to about 5%, from about 1% to about 4%, from about 1% to about 3%, from about 1% to about 2%, from about 2% to about 4%, from about 2% to about 3%, or from about 3% to about 4%.

In certain embodiments, the hemostatic hydrogel, when immersed in saline for about 8 hours exhibits a mass reduction of from about 6% to about 10%, from about 7% to about 10%, from about 8% to about 10%, from about 9% to about 10%, from about 6% to about 9%, from about 6% to about 8%, from about 6% to about 7%, from about 7% to about 9%, from about 7% to about 8%, or from about 8% to about 10%.

In certain embodiments, the hemostatic hydrogel, when immersed in saline for about 24 hours exhibits a mass reduction of from about 20% to about 25%, from about 21% to about 25%, from about 22% to about 25%, from about 23% to about 25%, from about 24% to about 25%, from about 20% to about 24%, from about 20% to about 23%, from about 20% to about 22%, from about 20% to about 21%, from about 21% to about 24%, from about 21% to about 23%, from about 21% to about 22%, from about 22% to about 24%, from about 22% to about 23%, or from about 23% to about 25%.

In certain embodiments, the hemostatic hydrogel, at least 30 seconds after formation, takes at least 5 minutes, 6 minutes, 7 minutes, 8 minutes, 9 minutes, 10 minutes, 11 minutes, 12 minutes, 13 minutes, 14 minutes, or 15 minutes to completely dissolve when exposed to a 5M hydroxylamine hydrochloride solution.

In certain embodiments, the hemostatic hydrogel, at least 60 seconds after formation, takes at least 6 minutes, 7 minutes, 8 minutes, 9 minutes, 10 minutes, 11 minutes, 12 minutes, 13 minutes, 14 minutes, 15 minutes, 16 minutes, or 17 minutes to completely dissolve when exposed to a 5M hydroxylamine hydrochloride solution.

In certain embodiments, the hemostatic hydrogel, at least 300 seconds after formation, takes at least 7 minutes, 8 minutes, 9 minutes, 10 minutes, 11 minutes, 12 minutes, 13 minutes, 14 minutes, 15 minutes, 16 minutes, 17 minutes, 18 minutes, 19 minutes, 20 minutes, 21 minutes, 22 minutes, 23 minutes, or 24 minutes to completely dissolve when exposed to a 5M hydroxylamine hydrochloride solution.

In certain embodiments, the hemostatic hydrogel, at least 1200 seconds after formation, takes at least 11 minutes, 12 minutes, 13 minutes, 14 minutes, 15 minutes, 16 minutes, 17 minutes, 18 minutes, 19 minutes, 20 minutes, 21 minutes, 22 minutes, 23 minutes, 24 minutes, 25 minutes, 26 minutes, 27 minutes, 28 minutes, 29 minutes, or 30 minutes to completely dissolve when exposed to a 5M hydroxylamine hydrochloride solution.

In certain embodiments, the hemostatic hydrogel, at least 1800 seconds after formation, takes at least 13 minutes, 15 minutes, 18 minutes, 21 minutes, 24 minutes, 27 minutes, 30 minutes, 33 minutes, or 36 minutes to completely dissolve when exposed to a 5M hydroxylamine hydrochloride solution.

In certain embodiments, the hemostatic hydrogel exhibits an increase in density at 2 hours, 3 hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours, or 24 hours after being immersed in the saline solution relative prior to immersion. In certain embodiments, the hemostatic hydrogel exhibits an increase in density at 4 hours after being immersed in the saline solution relative prior to immersion.

In certain embodiments, the hemostatic hydrogel permits Schiff base rearrangement thereby increasing the density of the crosslinked moieties of formula (IX). In certain embodiments, the number of crosslinked moieties of formula (IX) increases for at least about 24 hours after the formation of the hemostatic hydrogel composition.

In certain embodiments, the number of crosslinked moieties of formula (IX) increases for at least about 1 hour, 2 hours, 4 hours, 8 hours, 12 hours, 18 hours, or about 24 hours after the formation of the hemostatic hydrogel composition. In certain embodiments, the number of crosslinked moieties of formula (IX) increases for at least about 24 hours after the formation of the hemostatic hydrogel composition.

In certain embodiments, the density of crosslinked moieties of formula (IX) increases for at least about 1 hour, 2 hours, 4 hours, 8 hours, 12 hours, 18 hours, or about 24 hours after the formation of the hemostatic hydrogel composition. In certain embodiments, the density of crosslinked moieties of formula (IX) increases for at least about 24 hours after the formation of the hemostatic hydrogel composition.

VIII Methods of Treatment and Administration

It is understood that the hemostatic hydrogel compositions can be used to promote hemostasis in a variety of scenarios, for example, when the blood loss is caused by trauma, abrasion, or surgical or other medical intervention at the location.

In certain embodiments, the surgical intervention is selected from an arthroscopic procedure, a cardiac surgery, a cranial surgery, an endoscopic procedure, a laparoscopic procedure, an OB-GYN surgery, an organ surgery, a plastic surgery, a sinus procedure, a spinal surgery, a thoracic surgery, or a vascular surgery. In certain circumstances, the cranial surgery can comprise a procedure to remove a hematoma or a tumor. In certain embodiments, the surgical intervention is a minimally invasive surgery, an endoscopic procedure, a laparoscopic procedure, or an arthroscopic procedure. In other approaches, the hemostatic hydrogel compositions of the present invention can be used as a topical wound dressing, for example, for the treatment of burns.

It is understood that, when appropriate, the hemostatic hydrogel composition, when applied to the site, is capable of filling a cavity at the site without inducing compression of tissue surrounding the cavity when the hemostatic hydrogel composition is exposed to physiological fluid or a body fluid. This can be particularly important during brain or spinal surgery where swelling of the hemostat in these locations is undesirable as it can cause compression of surrounding tissue. In certain embodiments, the hemostatic hydrogel compositions described herein optionally further comprises an agent that enhances the rate of shrinkage of the hemostatic hydrogel composition and/or enhances the rate of hemostasis facilitated by the hemostatic hydrogel relative to a hemostatic hydrogel without the agent. In certain embodiments, the agent that enhances the rate of shrinkage of the hemostatic hydrogel is a salt. In certain embodiments, the salt comprises, for example, a monovalent cation, a bivalent cation, or a trivalent cation. In certain embodiments the salt is selected from the group consisting of sodium chloride, sodium iodide, potassium chloride, sodium alginate, magnesium chloride, calcium chloride, calcium alginate, a silver oxysalt, zinc chloride, zinc sulfate, ferrous sulfate, silver nitrate, aluminum sulfate, ferric sulfate, ferric chloride, and combinations thereof. In certain embodiments, the agent that enhances the rate of shrinkage of the hemostatic hydrogel composition may also enhance the rate of hemostasis facilitated by the hemostatic hydrogel relative to a hemostatic hydrogel without the agent.

In addition, it is understood that the hemostatic hydrogel can be used to facilitate the delivery of a therapeutic agent to a site of intent, for example, during surgery. In certain embodiments, the therapeutic agent is selected from the group consisting of a small molecule drug, a growth factor, a hormone, an antibody, an anti-cancer agent, an antimicrobial. In certain embodiments, the small molecule drug compound is selected from the group comprising an antibiotic, a non-steroidal anti-inflammatory agent.

In certain embodiments, the therapeutic agent can include, without limitation, a polynucleotide (e.g., DNA, RNA), an oligonucleotide, a gene therapy agent, a nucleoside analog (e.g., Cytovene, Epivir, Gemzar, Hivid, Rebetron, Videx, Zerit, Zovirax), a polynucleic acid decoy, a peptide (e.g., peptide hormone), a protein (e.g., a therapeutic antibody, e.g., Ig A, Ig G, Ig M, Ig D, and Ig E antibodies), or a growth factor (e.g., bone morphic growth factor (BMP), angiopoietin, acidic fibroblast growth factor (aFGF), basic fibroblast growth factor (bFGF), vascular endothelial growth factor (vEGF), platelet derived growth factor (PDGF), nerve growth factor (NGF)), an anti-inflammatory drug (e.g., dexamethasone), an immune suppressive agent, an anti-neoplastic agent, an anti-cancer agent, an anti-cell proliferation agent, a nitric oxide releasing agent, an anti-diabetic drug (e.g., rosigliatazone), an antibiotic (e.g., Minocycline, Rifampin, Erythromycin, Novobiocin), an anti-microbial agent (e.g., Triclosan, Fusidic acid, Silver acetate, Polymyxin), an analgesic (e.g., codeine, meperidine, morphine, aspirin, acetaminophen, d-propoxyphene), a burn care agent (e.g., silver sulfadiazine, bacitracin, benzocaine) or any combination thereof.

In certain embodiments, the method further comprising administering a plurality of cells, for example, immune cells, e.g., engineered immune cells (e.g., CAR T cells) or stem cells to the site. In certain embodiments, the hemostatic hydrogel composition comprises a plurality of stem cells. In certain embodiments, the plurality of stem cells comprise stem cells selected from mesenchymal stem cells, pancreatic stem cells, pluripotent stem cells, neural stem cells, hematopoietic stem cells or any combination thereof. In certain embodiments, the hemostatic hydrogel compositions of the present invention can be used to promote tissue regeneration.

In certain embodiments, when a hemostatic hydrogel composition of the present invention is applied to an abrasion, hemostasis is achieved, for example, from about 5 seconds to about 120 seconds, from about 10 seconds to about 120 seconds, from about 15 seconds to about 120 seconds, from about 5 seconds to about 60 seconds, from about 10 seconds to about 60 seconds, from about 15 seconds to about 60 seconds, from about 5 seconds to about 30 seconds, from about 10 seconds to about 30 seconds, from about 15 seconds to about 30 seconds, from about 5 seconds to about 15 seconds, or from about 10 seconds to about 15 seconds, after the hemostatic hydrogel composition is applied to the location. In certain embodiments, when a hemostatic hydrogel composition of the present invention is applied to an abrasion, hemostasis is achieved from about 10 seconds to about 40 seconds, after the hemostatic hydrogel composition is applied to the location.

In certain embodiments, when a hemostatic hydrogel composition of the present invention is applied to a biopsy punch, hemostasis is achieved, for example, from about 5 seconds to about 60 seconds, from about 10 seconds to about 60 seconds, from about 15 seconds to about 60 seconds, from about 20 seconds to about 60 seconds, from about 25 seconds to about 60 seconds, from about 30 seconds to about 60 seconds, from about 40 seconds to about 60 seconds, from about 50 seconds to about 60 seconds, from about 5 seconds to about 50 seconds, from about 5 seconds to about 40 seconds, from about 5 seconds to about 35 seconds, from about 5 seconds to about 30 seconds, from about 5 seconds to about 25 seconds, from about 5 seconds to about 20 seconds, from about 5 seconds to about 15 seconds, from about 5 seconds to about 10 seconds, from about 10 seconds to about 50 seconds, from about 10 seconds to about 40 seconds, from about 10 seconds to about 35 seconds, from about 10 seconds to about 30 seconds, from about 10 seconds to about 25 seconds, from about 10 seconds to about 20 seconds, from about 10 seconds to about 15 seconds, from about 15 seconds to about 50 seconds, from about 15 seconds to about 40 seconds, from about 15 seconds to about 35 seconds, from about 15 seconds to about 30 seconds, from about 15 seconds to about 25 seconds, from about 15 seconds to about 20 seconds, from about 20 seconds to about 50 seconds, from about 20 seconds to about 40 seconds, from about 20 seconds to about 35 seconds, from about 20 seconds to about 30 seconds, from about 20 seconds to about 25 seconds, from about 25 seconds to about 50 seconds, from about 25 seconds to about 40 seconds, from about 25 seconds to about 35 seconds, from about 25 seconds to about 30 seconds, from about 30 seconds to about 50 seconds, from about 30 seconds to about 40 seconds, from about 30 seconds to about 35 seconds, from about 35 seconds to about 50 seconds, from about 35 seconds to about 40 seconds, or from about 35 seconds to about 40 seconds, after the hemostatic hydrogel composition is applied to the location. In certain embodiments, when a hemostatic hydrogel composition of the present invention is applied to a biopsy punch, hemostasis is achieved in less than 30 seconds, for example, from about 10 seconds to about 20 seconds, after the hemostatic hydrogel composition is applied to the location.

In certain embodiments, when a hemostatic hydrogel composition of the present invention is applied to a laceration, hemostasis is achieved, for example, from about 10 seconds to about 100 seconds, from about 20 seconds to about 100 seconds, from about 30 seconds to about 100 seconds, from about 40 seconds to about 100 seconds, from about 50 seconds to about 100 seconds, from about 70 seconds to about 100 seconds, from about 90 seconds to about 100 seconds, from about 10 seconds to about 90 seconds, from about 10 seconds to about 70 seconds, from about 10 seconds to about 50 seconds, from about 10 seconds to about 40 seconds, from about 10 seconds to about 30 seconds, from about 10 seconds to about 20 seconds, from about 20 seconds to about 90 seconds, from about 20 seconds to about 70 seconds, from about 20 seconds to about 50 seconds, from about 20 seconds to about 40 seconds, from about 20 seconds to about 30 seconds, from about 30 seconds to about 90 seconds, from about 30 seconds to about 70 seconds, from about 30 seconds to about 50 seconds, from about 30 seconds to about 40 seconds, from about 40 seconds to about 90 seconds, from about 40 seconds to about 70 seconds, from about 40 seconds to about 50 seconds, from about 50 seconds to about 90 seconds, from about 50 seconds to about 70 seconds, or from about 70 seconds to about 90 seconds, after the hemostatic hydrogel composition is applied to the location.

In certain embodiments, when a hemostatic hydrogel composition of the present invention is applied to a laceration, hemostasis is achieved, for example, from about 10 seconds to about 90 seconds, after the hemostatic hydrogel composition is applied to the location. In certain embodiments, when a hemostatic hydrogel composition of the present invention is applied to a laceration, hemostasis is achieved from about 80 seconds to about 180 seconds, after the hemostatic hydrogel composition is applied to the location.

In certain embodiments, the hemostatic hydrogel composition is applied to the location in the form of a spray. In certain embodiments, the hemostatic hydrogel composition is applied to the location in the form of a flowable gel. In certain embodiments, the hemostatic hydrogel composition is applied to the location in the form of a liquid bandage.

It is understood that, depending upon the circumstances, it may be desirable to remove the hemostatic hydrogel composition from the subject after hemostasis. This may be achieved by exposing the hemostatic hydrogel composition to a dissolution agent that dissolves the hemostatic gel. The dissolution agent can be, for example, an organic compound comprising a primary amine, for example, a lysine, lysine hydrochloride, nicotinamide, thiamine hydrochloride, thiamine mononitrate, isopropylamine, or combinations thereof. In certain embodiments, the dissolution agent can be an organic compound comprising a primary amine that is capable of breaking Schiff base linkages.

Similarly, it is contemplated that a hemostatic hydrogel can be formed at a particular location in the subject to facilitate hemostasis. Following hemostasis, the hemostatic hydrogel can be removed, for example, by dissolution. The dissolution agent can be, for example, an organic compound comprising a primary amine, for example, a lysine, lysine hydrochloride, nicotinamide, thiamine hydrochloride, thiamine mononitrate, isopropylamine, or combinations thereof. In certain embodiments, the dissolution agent can be an organic compound comprising a primary amine that is capable of breaking Schiff base linkages.

Kits

In various embodiments, the invention provides kits for producing hemostasis (e.g., reducing or stopping blood loss) at a location in a subject in need thereof. In certain embodiments, a kit comprises: i) instructions for producing hemostasis at a location in a subject in need thereof, ii) an acrylated chitosan composition described herein, and/or iii) an oxidized dextran composition described herein, and an optional mixing system for mixing the acrylated chitosan and oxidized dextran and an optional dispensing system for dispensing a mixture of the acrylated chitosan and the oxidized dextran.

In certain embodiments, the kit comprises a container (for example, syringe, tube, or bottle) containing the acrylated chitosan composition described herein and a container (for example, syringe, tube or bottle) containing the oxidized dextran composition described herein in respective amounts sufficient to produce a hemostatic hydrogel for facilitating hemostasis at the location in the subject in need thereof. In certain embodiments, the kit comprises one or more containers of the acrylated chitosan composition and the oxidized dextran composition described herein in respective amounts sufficient to produce a hemostatic hydrogel for facilitating hemostasis at one or more locations in the subject in need thereof. In certain embodiments, the kit comprises the acrylated chitosan composition and the oxidized dextran composition described herein in amounts sufficient to produce hemostasis at 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 locations in the subject in need thereof.

EXAMPLES

The invention now being generally described, will be more readily understood by reference to the following examples, which are included merely for purposes of illustration of certain aspects and embodiments of the present invention, and are not intended to limit the invention.

Example 1 Method of Making an Exemplary Acrylated Chitosan Composition

This example describes a method for making an acrylated chitosan for use in creating a hemostatic hydrogel composition.

An exemplary acrylated chitosan was prepared as follows:

Step 1—Preparation of a Chitosan Intermediate

4.0 g of raw chitosan (Mw=162 kDa, PDI=2.3, DDA=79%) starting material was dissolved in 200 g of 1% (v/v) acetic acid solution for 30 minutes at 25° C. to produce a mixture. The mixture was then heated to 100° C. and held at this temperature for 2 hours.

Step 2—Preparation of the Acrylated Chitosan Intermediate

The mixture comprising the chitosan intermediate was then cooled to 50° C. Thereafter 5.3 g of acrylic acid was added and the mixture was then heated to 100° C. and held at this temperature for 60 minutes. The reaction was then cooled to 28° C. and then quenched by the addition of NaOH until a final pH value of 12.4 was achieved.

Step 3—Preparation of the Acrylated Chitosan Composition

The mixture comprising the acrylated chitosan intermediate was then purified by dialysis for 8 hours to remove salts and low molecular weight components from the mixture to achieve a pH value of 9.1. The purified acrylated chitosan was recovered by precipitation from isopropanol which resulted in a yield of 88%.

Finally, the material was characterized using ¹H-NMR spectroscopy and was determined that the mole fraction of the monomer of formula (III) was 0.37.

Example 2 Method of Making an Exemplary Acrylated Chitosan Composition

This example describes another method for making an acrylated chitosan for use in creating a hemostatic hydrogel composition.

An exemplary acrylated chitosan was prepared as follows:

Step 1—Preparation of a Chitosan Intermediate

4.009 g of raw chitosan (Mw=251 kDa, PDI=3.41, DDA=87.87%) starting material was dissolved in 200 g of 1% acetic acid solution (v/v) for about 14 hours at 25° C. to produce a mixture. The mixture was then heated to 100° C. and held at this temperature for 2 hours.

Step 2—Preparation of the Acrylated Chitosan Intermediate

The mixture comprising the chitosan intermediate was then cooled to 50° C. Thereafter 5.4 g of acrylic acid was added and the mixture was then heated to 100° C. and held at this temperature for 60 minutes. The reaction was then cooled to 28° C. and then quenched by the addition of NaOH until a final pH value of 12.81 was achieved.

Step 3—Preparation of the acrylated chitosan composition

The mixture comprising the acrylated chitosan intermediate was then purified by dialysis to remove salts and low molecular weight components from the mixture to achieve a pH value of 9.27. The purified acrylated chitosan was recovered by precipitation from isopropanol which resulted in a yield of 96.83%.

Finally, the material was then characterized using ¹H-NMR spectroscopy. It was determined that the mole fraction of the monomer of formula (III) was 0.412, the mole fraction of the monomer of formula (I) was 0.132, the mole fraction of the monomer of formula (II) was 0.441, and the mole fraction of the monomer of formula (IV) was 0.015.

Example 3 Method of Making an Exemplary Acrylated Chitosan Composition

This example describes a third method for making an acrylated chitosan for use in creating a hemostatic hydrogel composition.

An exemplary acrylated chitosan was prepared as follows:

Step 1—Preparation of a Chitosan Intermediate

4.002 g of raw chitosan (Mw=170 kDa, PDI=1.91, DDA=84.67%) starting material was dissolved in 200 g of 1% acetic acid solution (v/v) for about 14 hours at 25° C. to produce a mixture. The mixture was then heated to 100° C. and held at this temperature for 2 hours.

Step 2—Preparation of the Acrylated Chitosan Intermediate

The mixture comprising the chitosan intermediate was then cooled to 50° C. Thereafter 5.4 g of acrylic acid was added and the mixture was then heated to 100° C. and held at this temperature for 35 minutes. The reaction was then cooled to 28° C. and then quenched by the addition of NaOH until a final pH value of 13.06 was achieved.

Step 3—Preparation of the Acrylated Chitosan Composition

The mixture comprising the acrylated chitosan intermediate was then purified by dialysis to remove salts and low molecular weight components from the mixture to achieve a pH value of 9.29. The purified acrylated chitosan was recovered by precipitation from isopropanol which resulted in a yield of 90.78%.

Finally, the material was characterized using ¹H-NMR spectroscopy. It was determined that the mole fraction of the monomer of formula (III) was 0.322, the mole fraction of the monomer of formula (I) was 0.145, the mole fraction of the monomer of formula (II) was 0.520, and the mole fraction of the monomer of formula (IV) was 0.013.

Example 4 Method of Making an Exemplary Oxidized Dextran Composition

This example describes a method for making an oxidized dextran for use in creating a hemostatic hydrogel composition.

An exemplary oxidized dextran was prepared as follows:

Step 1—Preparation of the Oxidized Dextran Intermediate

A dextran solution was prepared by dissolving 5.0 g of raw dextran starting material (Mw=129 kDa, PDI=4.58) in 400 g of distilled water for 30 minutes at 25° C. Thereafter a sodium periodate solution was prepared by dissolving 3.28 g of sodium periodate in 50 g of distilled water. The sodium periodate solution was then added to the dextran solution and the resulting mixture was stirred for 24 hours.

Step 2—Preparation of the Oxidized Dextran Composition

The mixture comprising the oxidized dextran intermediate was then purified by dialysis for 8 hours in order to remove salts and low molecular weight components from the mixture. The purified oxidized dextran was recovered by precipitation from ethanol which resulted in a yield of 88%.

The total amount of aldehyde groups present on the oxidized dextran was measured using the following titration method:

150 mg of oxidized dextran was added to 35 mL of hydroxylamine hydrochloride solution and allowed to stir for 24 hours at room temperature. This solution was titrated with a NaOH solution. The titration was followed potentiometrically, with the pH recorded as a function NaOH volume. The volume of NaOH solution used to titrate the oxidized dextran solution was taken to be the endpoint, which was determined as the inflection point of the titrimetric curve.

The total amount of aldehyde groups present on the oxidized dextran was found to be 0.76 mol. aldehyde/mol. dextran.

Example 5 Method of Making an Exemplary Oxidized Dextran Composition

This example describes a second method for making an oxidized dextran for use in creating a hemostatic hydrogel composition.

An exemplary oxidized dextran was prepared as follows:

Step 1—Preparation of the Oxidized Dextran Intermediate

A dextran solution was prepared by dissolving 5.0 g of raw dextran starting material (Mw=129 kDa, PDI=4.58) in 400 g of distilled water for about 30 minutes at 25° C. Thereafter a sodium periodate solution was prepared by dissolving 3.3 g of sodium periodate in 50 g of distilled water. The sodium periodate solution was then added to the dextran solution and stirred. The oxidation reaction was complete in about 1.5 hours.

Step 2—Preparation of the Oxidized Dextran Composition

The mixture comprising the oxidized dextran intermediate was then concentrated 2-fold to a solution weight of about 207.5 g and then purified for about 6 hours using ultrafiltration to remove salts and low molecular weight oxidized dextran chains from the mixture. The purified oxidized dextran was then recovered by precipitation from ethanol, which resulted in a yield of 63.1%.

At the end of the oxidation reaction, the formic acid content was determined as follows: 25 mL of the oxidized dextran solution was collected and titrated against 0.01M NaOH using a phenolphthalein solution as the indicator. The formic acid content was then used to quantify the number of secondary aldehydes present in the oxidized dextran solution using the formula: secondary aldehydes=2× formic acid content

A second titration to determine the total amount of aldehyde groups present on the oxidized dextran was performed as follows:

150 mg of oxidized dextran was added to 35 mL of hydroxylamine hydrochloride solution and allowed to stir for 24 hours at room temperature. This solution was then titrated with a NaOH solution. The titration was followed potentiometrically, with the pH recorded as a function NaOH volume. The volume of NaOH solution used to titrate the oxidized dextran solution was taken to be the endpoint, which was determined as the inflection point of the titrimetric curve.

The total amount of aldehyde groups present in the oxidized dextran was determined to be 0.79 mol. aldehyde/mol. dextran. The primary to secondary aldehyde ratio was then calculated using the total aldehyde and secondary aldehyde content and was found to be 1.54.

It was determined that the mole fraction of monomer (V) was 0.6026, the mole fraction of monomer VI and/or monomer VII was 0.2411, and the mole fraction of monomer VIII was 0.1564.

Example 6 Method of Making an Exemplary Hemostatic Hydrogel Composition

This example describes a method for making a hemostatic hydrogel composition for use in reducing/stopping bleeding at a tissue lesion.

An exemplary hemostatic hydrogel composition was prepared as follows:

The acrylated chitosan of Example 1 and oxidized dextran of Example 4 were each solubilized into a buffered saline solution to give a final concentration of 7.5% (w/w) and 7.5% (w/w), respectively. Equal amounts of the aqueous solution of the oxidized dextran provided in Example 4 (concentration: 7.5% w/w) and the aqueous solution of acrylated chitosan provided in Example 1 (concentration: 7.5% w/w) were loaded in a dual barrel syringe. A mixer was attached to the top of the dual barrel syringe. The two solutions were then passed through the mixer simultaneously. The hydrogel was observed to form instantaneously at the tip of the mixer. The combined solution was further aerosolized under pressure.

The burst strength of the acrylated chitosan/oxidized dextran hydrogel was measured using ASTM F 2392-04 and found to be 96±11 mmHg (C.I of 95%).

Example 7 Characterization of the Structural Properties of an Exemplary Hemostatic Hydrogel

This example describes the characterization of the structural property in an exemplary hemostatic hydrogel.

An acrylated chitosan composition was produced essentially as described in Example 1 and an oxidized dextran composition was prepared essentially as described in Example 4. When combined essentially as described in Example 6, the structural property was analyzed using Scanning Electron Microscopy (SEM).

The structure of the acrylated chitosan/oxidized dextran hydrogels were analyzed using SEM (see, FIG. 1). The hydrogels were found to have formed a three-dimensional layered structure comprising, substantially non-interconnected anisotropic cells/pores formed between the hydrogel backbone walls. The layers of cells/pores were staggered and substantially non-inter connected with layers directly above and below. As a result, the hydrogels could capture cells (e.g., platelets, red blood cells) and prevent them from passing through and exiting the hydrogel structure.

Example 8 Characterization of the Elastic Modulus of an Exemplary Hemostatic Hydrogel

This example describes the characterization of the elastic modulus in an exemplary hemostatic hydrogel.

An acrylated chitosan composition was produced essentially as described in Example 1 and an oxidized dextran composition was prepared essentially as described in Example 4. When combined essentially as described in Example 6, the elastic modulus was measured using a rheometer. The results are presented in FIG. 3.

The data in FIG. 3 shows that the acrylated chitosan/oxidized dextran hydrogel achieved a desired stiffness of greater than 500 Pa that increases over time; which is required for the hemostatic hydrogel to exert an initial tamponade effect when applied to a wound.

Example 9 Characterization of the Gelation Time of an Exemplary Hemostatic Hydrogel

This example describes the characterization of the gelation time of an exemplary hemostatic hydrogel.

An acrylated chitosan composition was produced essentially as described in Example 1 and an oxidized dextran composition was prepared essentially as described in Example 4. When combined essentially as described in Example 6, the gelation time was measured using stir bar stop test. The gelation time was found to be 8 seconds. This example shows that the exemplary hemostatic hydrogel forms quickly, which is important in achieving fast hemostasis.

Example 10 The Effect of Different Concentrations of Acrylated Chitosan and Oxidized Dextran Precursor Solutions on the Gelation Time of Exemplary Hemostatic Hydrogels

This example describes the effect of different concentrations of acrylated chitosan and oxidized dextran precursor solutions on the gelation time of exemplary hemostatic hydrogels.

Acrylated chitosan precursor solutions of varying concentration were produced essentially as described in Example 1, oxidized dextran precursor solutions were prepared essentially as described in Example 4, and combined essentially as described in Example 6 to produce the hydrogels.

Gelation times were measured using two techniques: 1) the stir bar test and 2) rheology.

1) Hydrogel Gelation Times Measured by the Stir Bar Test

The gelation times of the hydrogels produced by differing concentrations of acrylated chitosan and oxidized dextran precursor solutions are shown in Table 1. The gelation time was determined to be the time taken for the stir bar to stop rotating or start deflecting in the hydrogel.

TABLE 1 Range of Average Conc. Acrylated Conc. Oxidized Gelation Gelation Chitosan Dextran Number Times Time (% (w/w)) (% (w/w)) of Tests (seconds) (seconds) 7 7 65 2-9 4.4 6 6 27  2-16 7.9 7 5 3 10-11 10.3 7 9 3 2 2

2) Hydrogel Gelation Times Measured by Rheology

Rheological measurements of hydrogels produced using acrylated chitosan and oxidized dextran precursor solutions of differing concentrations were collected at 25° C. using a HAAKETM Rheostress 600 rheometer (Thermo Scientific).

Solution concentrations of 2% (w/w) and 7% (w/w) of the precursor solutions were used to prepare the hydrogels. FIG. 4 and FIG. 5 show the changes in elastic storage modulus (G′) and viscous loss modulus (G″) curves as a function of time for the hydrogels produced by the 2% (w/w) and 7% (w/w) precursor solutions, respectively.

In this assay, gelation time is calculated based upon the time at which the G′ and G″ curves cross over.

As can be seen in FIG. 4 the G′ and G″ curves crossed over about 85 seconds after the initial mixing of the 2% (w/w) precursor solutions.

FIG. 5 shows that the G′ and G″ curves had already crossed over prior to the first rheological measurement being taken at about 30 seconds after the initial mixing of the 7% (w/w) precursor solutions. This indicated that the gelation time for the hydrogel was less than about 30 seconds.

For a typical gel-based material, upon completion of gelation it is expected that G′ will reach equilibrium and G″ approaches 0. However, it was observed that at both precursor concentrations the values of G′ and G″ continued to increase over time, which is indicative of a hydrogel material with dynamic properties. It is contemplated that the dynamic nature of the hydrogels maybe due to an increasing number of Schiff base bonds forming between acrylated chitosan and oxidized dextran as a function of time.

Example 11 Characterization of the Rate of Shrinkage of an Exemplary Hemostatic Hydrogel

This example describes the characterization of the rate of shrinkage of an exemplary hemostatic hydrogel.

An acrylated chitosan composition was produced essentially as described in Example 1 and an oxidized dextran composition was prepared essentially as described in Example 4. When combined essentially as described in Example 6, the rate of shrinkage was measured as function of weight loss over time. The rate of shrinkage of the hydrogel is shown in FIG. 6, which demonstrates that the hydrogel shrinks, rather than swells, overtime. This feature is particularly helpful when a hemostat is used to stop bleeding in confined spaces (e.g., a cranium or a spine) without compressing the nearby tissue.

Example 12 Effect of Environment on the Rate of Shrinkage of the Exemplary Hemostatic Hydrogels

This example describes the effect of environment on the rate of shrinkage of the exemplary hemostatic hydrogels.

Acrylated chitosan compositions were produced essentially as described in Example 1, oxidized dextran compositions were prepared essentially as described in Example 4, and combined essentially as described in Example 6 to produce the hydrogels.

The rate of shrinkage of the hydrogels was measured in 3 different environments: 1) moist environment, room temperature, and 2) complete immersion in a saline solution.

1) Moist Environment, Room Temperature

The hydrogel was formed over a collagen support. The hydrogel with the collagen support was then placed on top of a wire mesh and this set up was then added to a container partially filled with water such that the hydrogel was suspended above the level of the water. The container was then placed under a digital microscope and the diameter of the hydrogel was measured at 2 minute intervals over a period of about 2 hours.

The shrinkage was measured as a function in the reduction in the diameter of the hydrogel. The shrinkage of the hydrogel is shown in FIG. 7, which demonstrates that the diameter of the hydrogel shrinks about 6.4% in about 2 hours.

2) Immersion in a Saline Solution

Two hydrogel compositions (Hydrogel A and Hydrogel B) were prepared by mixing 1.2 mL of a 7% (w/w) acrylated chitosan solution with 1.2 mL of a 7% (w/w) oxidized dextran solution using a 16 element static mixer and dispensing the mixture into a cylindrical mold (height=8.03 mm, diameter=14.96 mm). Hydrogels A and B were then removed from the molds 2 minutes after dispensing. The weight of the hydrogel samples was then measured before completely immersing each sample in Blood Bank saline solution at room temperature for a period of 60 days.

The rate of shrinkage was determined by monitoring the weight loss (loss of water) of the hydrogels as a function of time (TABLE 2 AND FIG. 8). Hydrogel A was determined to shrink about 70% over 60 days. Hydrogel B was determined to shrink about 65% over 49 days.

TABLE 2 Hydrogel A Hydrogel B Weight % reduction Weight % reduction Time (g) in weight Time (g) in weight 2 mins 1.317 0 2 mins 1.3649 0 15 mins 1.319 −0.1% 15 mins 1.4003 −2.59% 30 mins 1.322 −0.4% 30 mins 1.4009 −2.64% 45 mins 1.318 −0.1% 45 mins 1.4042 −2.88% 60 mins 1.317 0.0% 60 mins 1.3967 −2.33% 2 hrs 1.304 1.0% 2 hrs 1.3894 −1.80% 4 hrs 1.278 3.0% 4 hrs 1.3518 0.96% 6 hrs 1.231 6.5% 6 hrs 1.3173 3.49% 8 hrs 1.187 9.9% 8 hrs 1.281 6.15% 24 hrs 0.986 25.2% 24 hrs 1.068 21.75% 48 hrs 0.814 38.2% 48 hrs 0.8813 35.43% 72 hrs 0.727 44.8% 72 hrs 0.7843 42.54% 4 days 0.663 49.7% 4 days 0.7209 47.18% 5 days 0.628 52.4% 5 days 0.6835 49.92% 6 days 0.588 55.3% 6 days 0.6403 53.09% 7 days 0.564 57.2% 7 days 0.6136 55.04% 8 days 0.548 58.4% 8 days 0.5905 56.74% 9 days 0.529 59.9% 9 days 0.5761 57.79% 10 days 0.520 60.5% 10 days 0.559 59.04% 13 days 0.491 62.7% 13 days 0.5333 60.93% 14 days 0.475 63.9% 14 days 0.527 61.4% 15 days 0.468 64.5% 15 days 0.521 61.9% 16 days 0.466 64.7% 16 days 0.519 62.0% 17 days 0.461 65.0% 17 days 0.512 62.5% 23 days 0.449 65.9% 23 days 0.498 63.5% 24 days 0.445 66.2% 24 days 0.491 64.0% 25 days 0.445 66.2% 25 days 0.489 64.2% 28 days 0.437 66.8% 28 days 0.486 64.4% 29 days 0.440 66.6% 29 days 0.480 64.8% 30 days 0.431 67.3% 30 days 0.480 64.8% 31 days 0.431 67.3% 31 days 0.479 64.9% 32 days 0.427 67.6% 32 days 0.475 65.2% 35 days 0.428 67.5% 35 days 0.472 65.4% 36 days 0.427 67.6% 36 days 0.471 65.5% 37 days 0.425 67.8% 37 days 0.470 65.5% 38 days 0.425 67.8% 38 days 0.468 65.7% 39 days 0.425 67.8% 39 days 0.468 65.7% 42 days 0.423 67.9% 42 days 0.466 65.8% 43 days 0.419 68.2% 43 days 0.464 66.0% 44 days 0.420 68.1% 44 days 0.461 66.2% 45 days 0.418 68.3% 45 days 0.461 66.2% 46 days 0.419 68.2% 46 days 0.461 66.2% 49 days 0.417 68.4% 49 days 0.461 66.2% 50 days 0.417 68.4% 50 days N/A N/A 51 days 0.416 68.4% 51 days N/A N/A 52 days 0.415 68.5% 52 days N/A N/A 53 days 0.413 68.6% 53 days N/A N/A 56 days 0.409 69.0% 56 days N/A N/A 57 days 0.408 69.0% 57 days N/A N/A 58 days 0.407 69.1% 58 days N/A N/A 59 days 0.407 69.1% 59 days N/A N/A 60 days 0.406 69.2% 60 days N/A N/A

Example 13 Effect of Shrinkage on the Pore Size of Exemplary Hemostatic Hydrogels

This example describes the effect of shrinkage on the pore size of exemplary hemostatic hydrogels.

Acrylated chitosan compositions were produced essentially as described in Example 1, oxidized dextran compositions were prepared essentially as described in Example 4, and combined essentially as described in Example 6 to produce the hydrogels.

A hydrogel after formation was analyzed by SEM (t=0 days). A second hydrogel prepared using the same materials and conditions was then completely immersed in Blood Bank saline solution (0.85% (w/v) NaCl) at room temperature for 107 days. The second hydrogel was then removed and analyzed by SEM. Representative SEM images of the hydrogel samples at t=0 days and t=107 days are shown in FIG. 9.

The pore size distribution of the hydrogel at t=0 days and t=107 days was calculated by analyzing the SEM images obtained for the two hydrogel samples using Image J software. It was observed that there was a reduction of about 85% in the average pore size of the hydrogel after 107 days of immersion in saline solution (TABLE 3). The pore size distribution was also observed to decrease (FIG. 10).

TABLE 3 % difference t = 0 days t = 107 days in pore size Number of Pores 396 96 N/A Measured Average Pore Size (μm) 161 20 88 Min. Pore Size (μm) 12 2 83 Max. Pore Size (μm) 807 83 90

Example 14 Effect of the Addition of Salts on the Rate of Shrinkage of Exemplary Hemostatic Hydrogels

This example describes the effect of the addition of salts on the rate of shrinkage of exemplary hemostatic hydrogels.

Acrylated chitosan compositions were produced essentially as described in Example 1, oxidized dextran compositions were prepared essentially as described in Example 4, and combined essentially as described in Example 6 to produce the hydrogels.

Aqueous solutions of NaCl with concentrations of 0.85% (w/w) and 33% (w/w) were prepared. Similarly, an aqueous solution of CaCl₂ with a concentration of 33% (w/w) was also prepared. Oxidized dextran was then dissolved in each of these solutions prior to mixing with the acrylated chitosan compositions to produce the hydrogels.

The rate of shrinkage of the hydrogels was measured as a function of weight loss over time (FIG. 11). It was observed that increasing the concentration of the salt in the hydrogel and using a bivalent cation increased the rate of shrinkage.

Example 15 Characterization of the Adhesion Strength of an Exemplary Hemostatic Hydrogel

This example describes the characterization of the adhesion properties of an exemplary hemostatic hydrogel.

An acrylated chitosan composition was produced essentially as described in Example 1 and an oxidized dextran composition was prepared essentially as described in Example 4. When combined essentially as described in Example 6, the adhesion strength was measured using ASTM F 2392-04 and found to be in the range from 16 to 27N. This example shows that the exemplary hemostatic hydrogel has enough strength to adhere to tissue and function as a hemostat.

Example 16 Method of Reducing/Stopping Bleeding Using an Exemplary Hemostatic Hydrogel Composition

This example describes a method for reducing/stopping bleeding using an exemplary hemostatic hydrogel composition. In the following studies, the exemplary hemostat was created essentially as described in Example 6, using the acrylated chitosan and oxidized dextran prepared as essentially described in Examples 1 and 4, respectively.

a) High Flow, Low Pressure Model—Liver (Abrasion Wounds)

In this example, the creation of wounds in a porcine liver was used a standard model to evaluate the effect of the acrylated chitosan/oxidized dextran hydrogel on hemostasis. A Teflon template with a 2 cm diameter circular cut-out to standardize the size of the abrasion wounds was used. The wound was created by swiping a Bovie scratch pad 5 times over the liver exposed in the template cut-out. The Bovie scratch pad created a bleeding effect similar to that found in human brain surgery. The bleeding wound was then blotted with dry gauze before the acrylated chitosan/oxidized dextran hydrogel was applied to the wound.

The transparent hydrogel adhered to the liver tissue and stopped blood flow immediately. The time to hemostasis was found to be 19±6 seconds (C.I of 95%). Complete coagulation (formation of a clot) occurred in 103±36 seconds (C.I of 95%). The formation of a clot was later verified using SEM (see, FIG. 12). FIG. 12 shows the aggregation of activated platelets within a pore. Dendritic pseudopodia of multiple platelets were observed, demonstrating platelet activation.

b) High Flow, High Pressure Model—Liver (Biopsy Punch)

A 10 mm diameter biopsy punch was plunged into a porcine liver, creating a circular wound, 10 mm in diameter and 5-10 mm in depth. Bleeding was observed to occur immediately. The tissue plug created by the punch was removed with forceps to create an open wound with high volume, high pressure bleeding. The wound was blotted with dry gauze, and the acrylated chitosan/oxidized dextran hydrogel was filled into the wound cavity, as well as being applied over the wound surface.

The transparent hydrogel adhered to the tissue and stopped blood flow immediately. The time to hemostasis was found to be between 14 to 18 seconds. The formation of a clot was later verified using SEM (see, FIG. 13).

c) High Flow, High Pressure Model—Liver (Laceration)

A scalpel was used to create lacerations in a porcine liver, the approximate dimensions of the lacerations were 30mm long×16mm deep. High flow rate, high pressure bleeding was observed to occur immediately. The wound area was blotted with dry gauze to remove excess blood and allow for visibility. The acrylated chitosan/oxidized dextran hydrogel was filled into the wound cavity, as well as being applied over the wound surface.

The transparent hydrogel adhered to the tissue and stopped blood flow immediately. The time to hemostasis was found to be 12 seconds. The formation of a clot was later verified using SEM (see, FIG. 14).

d) High Flow, High Pressure Model—Spleen (Laceration)

The spleen was used as a model to evaluate the effect of the acrylated chitosan/oxidized dextran hydrogel on hemostasis as the spleen is a well vascularized organ that can bleed profusely. A scalpel was used to lacerate the spleen, resulting in lacerations that were 30mm long×16mm deep. The wound was then blotted with dry gauze to remove excess blood and allow for visibility. The acrylated chitosan/oxidized dextran hydrogel was filled into the wound cavity, as well as applied over the wound surface.

The organ was picked up and observed visually to determine that blood flow had stopped and that hemostasis had been achieved. The time to hemostasis was found to be 82 seconds. The formation of a clot was later verified using SEM (see, FIG. 15).

FIG. 15 shows a thick network of fibrin strands trapping multiple activated platelets and red blood cells. Dendritic pseudopodia of multiple platelets was observed, demonstrating platelet activation.

Example 17 Comparative Study I—Analysis of Acrylated Chitosan and Resulting Hemostatic Hydrogels

This example describes a comparison of the properties of exemplary acrylated chitosan compositions described herein and hemostatic hydrogel compositions produced using such acrylated chitosan compositions relative to the acrylated chitosan compositions and hemostatic hydrogel compositions prepared using the methods described in U.S. Pat. No. 7,854,923 (the '923 Patent).

In the following studies, exemplary hemostatic hydrogel compositions were created essentially as described in Example 6, using the acrylated chitosan and oxidized dextran compositions prepared as essentially described in Examples 1 and 4, respectively. For the comparison, hydrogel compositions were created essentially as described in Example 8 of the '923 Patent, using the acrylated chitosan and oxidized dextran compositions prepared as essentially described therein in Examples 1 and 6, respectively.

1) Acrylated Chitosan Compositions

SEC-MALS using the ASTM F2602-08 protocol was used to determine the Mz values of acrylated chitosan samples prepared using the two different approaches. The Mz value of the starting, raw chitosan was 952 kDa. The Mz of the acylated chitosan produced by Example 1 of the '923 Patent was 1,077 kDa (in other words, larger than the starting raw chitosan). In contrast, the Mz of the acrylated chitosan produced by the method described herein was 610 kDa (in other words, smaller than the starting raw chitosan).

The acrylated chitosan produced using the approach of the '923 Patent was a heterogenous mixture of multiple, separate components defined by at least two distinct peaks (a bimodal distribution) as determined by SEC-MALS (solid line). In contrast, the acrylated chitosan produced by the method described herein was a more uniform, homogenous material as defined by a single peak with a small shoulder (a unimodal distribution) as determined by SEC-MALS (dotted line). An overlay of the resulting spectra is presented in FIG. 16.

In addition, ¹H NMR was conducted on the samples produced by each method, which indicated that the acrylated chitosan produced by the two methods was different. ¹H-NMR was performed essentially as described in Lavertu, et al. (Lavertu et al. (2003) J. PHARM. BIOMED. ANALYSIS, 32: 1149-1158.) using a 400 MHz Bruker instrument (Billerica, Mass.). Data acquisition was performed using the Bruker TopSpin™ software and zg30 Proton Pulse program. Comparison of the ¹H-NMR spectra corresponding to the acrylated chitosan produced by the two methods revealed that the composition of the resulting acrylated chitosan preparations were chemically different. Among other things, the peaks corresponding to the undesirable diacrylated monomer (AC-2, monomer of formula IV) were significantly larger in the acrylated chitosan made by the method of the '923 Patent. It was calculated that the mole fraction of the AC-2 monomer in the preparation of the '923 Patent was 0.028, whereas the mole fraction of the AC-2 monomer in the preparation described herein was 0.017.

2) Hydrogel Compositions

The gelation times of the gels produced using the materials described herein, including the acrylated chitosan produced using an acetic acid step, are faster than those achieved using the material of the '923 Patent. The gelation times reported in Example 8 of the '923 Patent were in the range of 30 seconds to 10 minutes. In contrast, the hydrogels created using the materials described herein, including the acrylated chitosan created with our pre-treatment step with organic acid (e.g., acetic acid), formed in less than 10 seconds, typically less than 2 seconds. In addition, when burst strengths of the hydrogels were measured using a method based on the ASTM F 2392 protocol, the average burst strength of the hydrogel described herein was about 85 mmHg, whereas the average burst strength of the hydrogel created by the method of the '923 Patent was about 18 mmHg.

Example 18 Comparative Study II—Dissolution of Exemplary Hemostatic Hydrogels

This example describes a comparison of the dissolution rates of exemplary hemostatic hydrogel compositions relative to the hemostatic hydrogel compositions prepared using the methods described in U.S. Pat. No. 7,854,923 (the '923 Patent) in 5M aqueous hydroxylamine hydrochloride (HHCl) solutions.

In the following studies, exemplary hemostatic hydrogel compositions were created essentially as described in Example 6, using the acrylated chitosan and oxidized dextran compositions prepared as essentially described in Examples 1 and 4, respectively. For the comparison, hydrogel compositions were created essentially as described in Example 8 of the '923 Patent, using the acrylated chitosan and oxidized dextran compositions prepared as essentially described therein in Examples 1 and 6, respectively.

The same raw chitosan and dextran materials were used to prepare both the exemplary hemostatic hydrogel compositions and the hemostatic hydrogel compositions prepared using the methods described in the '923 patent.

The concentration of the acrylated chitosan and oxidized dextran compositions used to create the exemplary hemostatic hydrogel compositions and those prepared using the methods described in the '923 patent were 4% (w/w). Five different samples of the exemplary hemostatic hydrogel compositions were prepared by allowing the hydrogel to cure for 30 seconds, 60 seconds, 300 seconds, 1,200 seconds and 1,800 seconds prior to dissolution testing.

Five different samples of the hemostatic hydrogel compositions produced using the methods described in the '923 patent were prepared by allowing the hydrogel to cure for 30 seconds, 60 seconds, 300 seconds, 1,200 seconds and 1,800 seconds prior to dissolution testing.

For dissolution testing, each hydrogel sample was added to 10 mL of 5M HHCl at room temperature. The HHCl solutions were stirred during dissolution and the time for complete dissolution of each hydrogel sample was determined visually.

It was observed that for each curing time (the time after the acrylated chitosan and oxidized dextran solution were mixed), the rate of dissolution of the exemplary hydrogel was slower than that for the reference hydrogel produced using the methods described in the '923 patent (TABLE 4 and FIG. 17).

TABLE 4 Curing Reference hydrogel Exemplary hydrogel time (secs) Time to dissolution (secs) Time to dissolution (secs) 30 183 362 60 210 418 300 246 458 1,200 347 692 1,800 312 780

It is contemplated that the slower dissolution rate of the exemplary hydrogel compared to the reference hydrogel is due to the formation of a denser matrix of Schiff base linkages with the hydrogel. In addition, as can be seen in FIG. 17, the time to complete dissolution for the reference hydrogel reached a maximum value of about 300 seconds when using curing times of greater than 1,200 seconds. It is contemplated that this dissolution behavior results from the hydrogel reaching steady-state (e.g., no further increase in the number of Schiff base linkages between the acrylated chitosan and oxidized dextran). In contrast, the time to complete dissolution of the exemplary hydrogel did not reach a maximum value over the same time period, but rather continued to increase, which may be because of an increase in the number and density of Schiff base linkages between the acrylated chitosan and oxidized dextran.

Example 19 Dissolution Rate of Exemplary Hemostatic Hydrogel Compositions Containing 7% (w/w) Acrylated Chitosan and 7% (w/w) Oxidized Dextran

This example shows the dissolution of a hemostatic hydrogel in 5M aqueous hydroxylamine hydrochloride (HHCl) solutions. The hydrogel was prepared as described in Example 6 by mixing 7% (w/w) acrylated chitosan prepared as in Example 1 with 7% (w/w) oxidized dextran prepared as in Example 4.

Five different samples of the exemplary hemostatic hydrogel composition were prepared by allowing the hydrogel to cure for 30 seconds, 60 seconds, 300 seconds, 1,200 seconds and 1,800 seconds prior to dissolution testing.

It was observed that that the time for complete dissolution to occur continually increased in a multi-phasic manner as a function of hydrogel curing time (see FIG. 18), which is believed to be due to an increase in the number and density of the Schiff base linkages between the acrylated chitosan and oxidized dextran as a function of time.

Incorporation by Reference

The entire disclosure of each of the patent documents and scientific articles referred to herein is incorporated by reference for all purposes.

Equivalents

The invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The foregoing embodiments are therefore to be considered in all respects illustrative rather than limiting the invention described herein. Scope of the invention is thus indicated by the appended claims rather than by the foregoing description, and all changes that come within the meaning and range of equivalency of the claims are intended to be embraced therein. 

We claim:
 1. An acrylated chitosan composition comprising acrylated chitosan comprising: (i) from about 0.01 to about 0.3 mole fraction of a first monomer of formula (I)

(ii) from about 0.3 to about 0.75 mole fraction of a second monomer of formula (II)

(iii) from about 0.2 to about 0.7 mole fraction of a third monomer of formula (III) and


2. The acrylated chitosan composition of claim 1, wherein the acrylated chitosan comprises from about 0.01 to about 0.26 mole fraction of the first monomer of formula (I).
 3. The acrylated chitosan composition of any one of claims 1-2, wherein the acrylated chitosan comprises from about 0.35 to about 0.65 mole fraction of the second monomer of formula (II).
 4. The acrylated chitosan composition of any one of claims 1-3, wherein the acrylated chitosan comprises from about 0.3 to about 0.6 mole fraction of the third monomer of formula (III).
 5. The acrylated chitosan composition of any one of claims 1-4, wherein the acrylated chitosan further comprises less than about 0.1 mole fraction of a fourth monomer of formula (IV)


6. The acrylated chitosan composition of any one of claims 1-5, wherein the acrylated chitosan has a weight-average molecular weight (Mw) of from about 25 kDa to about 400 kDa or from about 115 kDa to about 200 kDa.
 7. The acrylated chitosan composition of any one of claims 1-6, wherein the acrylated chitosan has a number-average molecular weight (Mn) of from about 14 kDa to about 200 kDa or from about 55 kDa to about 140 kDa.
 8. The acrylated chitosan composition of any one of claims 1-7, wherein the acrylated chitosan has a polydispersity index (PDI) of from about 1.5 (Mw/Mn) to about 3.5 (Mw/Mn).
 9. The acrylated chitosan composition of any one of claims 1-8, wherein the acrylated chitosan has a PDI of from about 1.5 (Mz/Mw) to about 7.0 (Mz/Mw), or from about 1.6 (Mz/Mw) to about 3.0 (Mz/Mw).
 10. The acrylated chitosan composition of any one of claims 1-9, wherein the acrylated chitosan composition comprises from about 1% (w/w) to about 25% (w/w), or from about 1% (w/w) to about 10% (w/w) of the acrylated chitosan.
 11. The acrylated chitosan composition of any one of claims 1-10, wherein the acrylated chitosan composition has a viscosity of from about 10 cP to about 50,000 cP, or from about 100 cP to about 25,000 cP.
 12. A method of preparing an acrylated chitosan composition comprising: (a) contacting a raw chitosan material with an aqueous organic acid solution to form a chitosan intermediate; (b) contacting the intermediate chitosan material with an α,β-unsaturated carboxylic acid to form an acrylated chitosan intermediate; and (c) purifying the acrylated chitosan intermediate thereby to produce the acrylated chitosan composition.
 13. The method of claim 12, wherein the acrylated chitosan composition produced in step (c) is the acrylated chitosan composition of any one of claims 1-11.
 14. The method of claim 12, wherein in step (a), contacting the raw chitosan material with the aqueous organic acid solution is conducted at a pressure of about 2 atmospheres.
 15. The method of any one of claims 12-13, wherein in step (a), the raw chitosan material is contacted with the aqueous organic acid solution at a temperature from about 80° C. to about 120° C.
 16. The method of any one of claims 12-14, wherein in step (a), the aqueous organic acid solution is a 1% (v/v) aqueous organic acid solution.
 17. The method of any one of claims 12-15, wherein in step (a), the aqueous organic acid solution is an acetic acid solution.
 18. The method of any one of claims 12-16, wherein in step (a), the PDI (Mw/Mn) of the chitosan intermediate is from about 15% to about 40% less than the PDI (Mw/Mn) of the raw chitosan material.
 19. The method of any one of claims 12-17, wherein in step (a), the raw chitosan material has a PDI of from about 1.5 (Mw/Mn) to about 5.0 (Mw/Mn).
 20. The method of any one of claims 12-18, wherein in step (a), the raw chitosan material has a degree of deacetylation of from about 65% to about 99% or from about 70% to about 98%.
 21. The method of any one of claims 12-19, wherein in step (b), the first chitosan intermediate is contacted with the α,β-unsaturated carboxylic acid at a temperature from about 50° C. to about 120° C.
 22. The method of any one of claims 12-20, wherein in step (b), the α,β-unsaturated carboxylic acid is selected from the group consisting of acrylic acid, butenoic acid, methacrylic acid, and combinations thereof.
 23. The method of any one of claims 12-21, the acrylated chitosan intermediate formed in step (b) has a degree of substitution (DS) value of from about 25% to about 65%.
 24. The method of any one of claims 12-22, further comprising the step of precipitating the acrylated chitosan composition to provide a solid.
 25. The method of claim 23, the method further comprising dissolving the solid into an aqueous medium to form a solution comprising an amount of the acrylated chitosan composition.
 26. The method of claim 24, wherein the amount of the acrylated chitosan composition in the solution is from about 1% to about 25%, or from about 1% to about 10% by weight of the total weight of the solution.
 27. An acrylated chitosan composition (for example, the acrylated chitosan composition of any one of claims 1-11) produced by the method of any one of claims 12-26.
 28. A method of preparing an acrylated chitosan composition comprising: (a) contacting a raw chitosan material with an acetic acid solution to form a chitosan intermediate, wherein the raw chitosan material has a PDI of from about 1.5 (Mw/Mn) to about 5.0 (Mw/Mn); (b) contacting the intermediate chitosan with acrylic acid to form an acrylated chitosan intermediate having a degree of substitution (DS) value of from about 25% to about 65%; and (c) purifying the acrylated chitosan intermediate thereby to produce the acrylated chitosan composition.
 29. The method of claim 28, wherein the acrylated chitosan composition produced in step (c) is the acrylated chitosan composition of any one of claims 1-11.
 30. The method of claim 26, further comprising the step of precipitating the acrylated chitosan composition produced in step (c) to provide a solid.
 31. The method of claim 27, further comprising the step of dissolving the solid into an aqueous medium to form a solution comprising from about 1% to about 10% acrylated chitosan composition (w/w) of the total weight of the solution.
 32. An acrylated chitosan composition (for example, the acrylated chitosan composition of any one of claims 1-11) produced by the method of any one of claims 28-31.
 33. An oxidized dextran composition comprising oxidized dextran comprising: (a) less than about 0.8 mole fraction of a first monomer of formula (V)

 and (b) from about 0.1 to about 1.0 mole fraction of a second monomer, wherein the second monomer is selected from a monomer of formula (VI), a monomer of formula (VII) and a combination of formula (VI) and formula (VII)


34. The oxidized dextran composition of claim 29, wherein the oxidized dextran comprises from about 0.4 to about 0.7 mole fraction of the first monomer of formula (V).
 35. The oxidized dextran composition of claim 29 or 30, wherein the oxidized dextran comprises from about 0.15 to about 0.35 mole fraction of the second monomer.
 36. The oxidized dextran composition of any one of claims 29-31, wherein the oxidized dextran further comprises less than about 0.65 mole fraction of a third monomer of formula (VIII)


37. The oxidized dextran composition of any one of claims 29-32, wherein the oxidized dextran has a Mw of from about 10 kDa to about 300 kDa or from about 15 kDa to about 90 kDa.
 38. The oxidized dextran composition of any one of claims 29-33, wherein the oxidized dextran has a Mn of from about 4 kDa to about 166 kDa or from about 4 kDa to about 45 kDa.
 39. The oxidized dextran composition of any one of claims 29-34, wherein the oxidized dextran has a PDI of from about 1.8 (Mw/Mn) to about 6.0 (Mw/Mn) or from about 2.0 (Mw/Mn) to about 4.0 (Mw/Mn).
 40. The oxidized dextran composition of any one of claims 29-35, wherein the oxidized dextran has a PDI of from about 1.5 (Mz/Mw) to about 6.0 (Mz/Mw) or from about 1.5 (Mz/Mw) to about 5.0 (Mz/Mw).
 41. The oxidized dextran composition of any one of claims 29-35, wherein the oxidized dextran comprises a total amount of aldehyde groups of from about 0.5 to about 2.0 or from about 0.6 to about 0.9 mol aldehydes/mol oxidized dextran.
 42. The oxidized dextran composition of any one of claims 29-41, wherein the ratio of primary aldehyde groups to secondary aldehyde groups is from about 1.5 to about 6.0 or from about 1.8 to about 3.5.
 43. The oxidized dextran composition of any one of claims 29-38, wherein the degree of oxidation is from about 25% to about 100% or from about 30% to about 50%.
 44. The oxidized dextran composition of any one of claims 29-39, wherein the oxidized dextran composition comprises from about 1% (w/w) to about 25% (w/w), or from about 1% (w/w) to about 10% (w/w) of the oxidized dextran.
 45. The oxidized dextran composition of any one of claims 29-39, wherein the oxidized dextran composition has a viscosity of from about 1 cP to about 2,000 cP, from about 1 cP to about 100 cP, or from about 1 cP to about 10 cP.
 46. A method of preparing an oxidized dextran composition, the method comprising the steps of: (a) contacting a solution comprising a raw dextran material with an oxidizing agent to form an oxidized dextran intermediate, wherein the concentration of the raw dextran material in the solution is greater than 1% (w/w); and (b) purifying the oxidized dextran intermediate thereby to produce an oxidized dextran composition.
 47. The method of claim 46, wherein the oxidized dextran composition produced in step (b) is the oxidized dextran composition of any one of claims 33-45.
 48. The method of claim 46 or 47, wherein during step (a), the concentration of the raw dextran material in the aqueous solution is at least 1.1% (w/w).
 49. The method of any one of claims 46-48, wherein during step (a), the raw dextran material has a Mw of from about 50 kDa to about 2,000 kDa.
 50. The method of claim any one of claims 46-49, wherein during step (a), the raw dextran material has a PDI of from about 1.4 (Mw/Mn) to about 5.0 (Mw/Mn).
 51. The method of any one of claims 46-50, wherein during step (a), the oxidizing agent is a periodate salt.
 52. The method of any one of claims 46-51, further comprising the step of precipitating the oxidized dextran composition to provide a solid.
 53. The method of claim 52, further comprising the step of dissolving the solid into an aqueous medium to form a solution comprising an amount of the oxidized dextran composition.
 54. The method of claim 53, wherein the amount of the oxidized dextran composition in the solution is from about 1% (w/w) to about 25% (w/w), or from about 1% (w/w) to about 10% (w/w) by weight of the total weight of the solution.
 55. An oxidized dextran composition (for example, the oxidized dextran composition of any one of claims 33-45) produced by the method of any one of claims 46-54.
 56. A hemostatic hydrogel composition containing oxidized dextran and acrylated chitosan, wherein the hydrogel composition comprises two or more of the following features: (i) a total amount of free aldehyde groups of from about 0.1 to about 0.7 moles aldehyde/mole oxidized dextran, (ii) the hemostatic hydrogel composition is formed from oxidized dextran and acrylated chitosan, wherein the ratio of primary aldehydes in the oxidized dextran to the amines in the acrylated chitosan is in the range from about 1.0 to about 2.0, and/or the ratio of total aldehydes in the oxidized dextran to amines in the acrylated chitosan is from about 1.5 to about 3.0, (iii) the ratio of Mw of the acrylated chitosan to the oxidized dextran is from about 2 to about 10, the ratio of Mn of the acrylated chitosan to the oxidized dextran is from about 4 to about 15, the ratio of Mz of the acrylated chitosan to the oxidized dextran is from about 2 to about 10, the ratio of PDI (Mw/Mn) of acrylated chitosan to oxidized dextran is from about 0.5 to about 0.8, and/or the ratio of PDI (Mz/Mw) of acrylated chitosan to oxidized dextran is from about 0.5 to about 1.0, (iv) upon formation of the hydrogel composition, the hydrogel composition comprises a bound water content of from about 65% w/w to about 95% w/w, (v) a three-dimensional porous structure comprising layers of substantially non-interconnected pores having (a) a pore size distribution from about 10 μm to about 850 μm in diameter, (b) a platelet adhesive surface, or a combination of (a) and (b), (vi) walls disposed between the substantially non-interconnected pores, the walls having a wall thickness of from 0.046 μm to 50 μm, (vii) a platelet adhesive surface so that, when in contact with blood, the hemostatic hydrogel composition permits platelets and/or red blood cells within the blood to adhere to platelet adhesive surface and promote blood clot formation at or within the hemostatic hydrogel composition, (viii) a platelet adhesive surface so that, when in contact with blood, the hemostatic hydrogel composition permits platelet and/or red blood cells within the blood to adhere to the platelet adhesive surface and not permit platelets and/or red blood cells from the blood to enter pores present in a first surface of the hemostatic hydrogel composition, pass through the hemostatic hydrogel composition, and then exit the hemostatic hydrogel composition via pores present in a second surface of the hemostatic hydrogel composition that opposes the first surface, (ix) at about 10 seconds after the formation of the hemostatic hydrogel composition, the hemostatic hydrogel composition has a burst strength of greater than 20 mmHg as determined using an ASTM F 2392-04 protocol, (x) at about 2 minutes after the formation of the hemostatic hydrogel composition, the hemostatic hydrogel composition has a burst strength of greater than about 35 mmHg as determined using an ASTM F 2392-04 protocol, (xi) at about 5 minutes after the formation of the hemostatic hydrogel composition, the hemostatic hydrogel composition has a burst strength of greater than about 70 mmHg as determined using an ASTM F 2392-04 protocol, (xii) an elastic modulus of from about 500 Pa to about 5000 Pa at from about 10 seconds to about 80 seconds after the formation of the hemostatic hydrogel composition, (xiii) a compression modulus of from about 3 kPa to about 250 kPa, (xiv) an average adhesion strength of from about 1.0 N to about 50.0 N, as determined using an ASTM F 2258-05 protocol, (xv) the volume of the hemostatic hydrogel composition, when formed, does not increase upon exposure to a physiological fluid or body fluid, (xvi) the volume of the hemostatic hydrogel composition shrinks by less than about 5% about 10 minutes after formation when exposed to a physiological fluid or body fluid, (xvii) the volume of the hemostatic hydrogel composition shrinks from about 5% to about 30% within about 2 hours after formation, from about 20% to about 60% within about 8 hours after formation, and from about 45% to about 70% within about 24 hours after formation, when exposed to a temperature of 37° C. and 75% relative humidity, (xviii) is substantially transparent when the hemostatic hydrogel composition has a thickness of 2 mm to 10 mm, and (xix) the hemostatic hydrogel composition optionally further comprises a therapeutic agent.
 57. The hemostatic hydrogel composition of claim 56, wherein the hydrogel comprises a gel produced by combining oxidized dextran with an acrylated chitosan composition produced by dissolving chitosan in an organic acid prior to acrylation.
 58. The hemostatic hydrogel composition of claim 57, wherein the organic acid is acetic acid.
 59. The hemostatic hydrogel composition of any one of claims 56-58, wherein the hemostatic hydrogel composition comprises a plurality of crosslinked moieties of formula (IX)


60. A hemostatic hydrogel composition comprising a gel produced by combining oxidized dextran with acrylated chitosan, wherein the hemostatic hydrogel composition comprises a plurality of crosslinked moieties of formula (IX)

and comprises one or more of the following features: (i) the hemostatic hydrogel, when immersed in saline for about 4 hours, exhibits a mass reduction of from about 1% to about 5%, (ii) the hemostatic hydrogel, when immersed in saline for about 8 hours, exhibits a mass reduction of from about 6% to about 10%, (iii) the hemostatic hydrogel, when immersed in saline for about 24 hours, exhibits a mass reduction of from about 20% to about 25%, (iv) the hemostatic hydrogel, when exposed to a physiological fluid or body fluid for about 8 hours, exhibits an irreversible decrease in volume, and (v) the hemostatic hydrogel, at least 30 seconds after formation, takes at least 5 minutes to completely dissolve when exposed to a 5M hydroxylamine hydrochloride solution.
 61. The hemostatic hydrogel composition of claim 60, wherein the hemostatic hydrogel exhibits an increase in density at 4 hours after being immersed in the saline solution relative prior to immersion.
 62. The hemostatic hydrogel composition of claim 60 or 61, wherein the hemostatic hydrogel permits Schiff base rearrangement thereby increasing the density of the crosslinked moieties of formula (IX).
 63. The hemostatic hydrogel composition of any one of claims 60-62, wherein the number of crosslinked moieties of formula (IX) increases for at least about 24 hours after the formation of the hemostatic hydrogel composition.
 64. The hemostatic hydrogel composition of any one of claims 60-63, wherein the density of crosslinked moieties of formula (IX) increases for at least about 24 hours after the formation of the hemostatic hydrogel composition.
 65. The hemostatic hydrogel composition of any one of claims 56-64 comprising: (a) from about 0.00 to about 0.3 mole fraction of a first monomer of formula (I)

(b) from about 0.02 to about 0.7 mole fraction of a second monomer of formula (III),

 and (c) from about 0.0 to about 0.8 mole fraction of a third monomer of formula (V),


66. The hemostatic hydrogel composition of any one of claims 56-65, wherein the hemostatic hydrogel composition comprises from about 0.0 to about 0.26 mole fraction of the first monomer of formula (I).
 67. The hemostatic hydrogel composition of any one of claims 56-66, wherein the hemostatic hydrogel composition comprises from about 0.03 to about 0.6 mole fraction of the second monomer of formula (III).
 68. The hemostatic hydrogel composition of any one of claims 56-67, wherein the hemostatic hydrogel composition comprises from about 0.04 to about 0.7 mole fraction of the third monomer of formula (V).
 69. The hemostatic hydrogel composition of any one of claims 56-68, wherein the hemostatic hydrogel composition comprises no greater than about 0.2 mole fraction of a fourth monomer of formula (IV)


70. The hemostatic hydrogel composition of any one of claims 56-69, wherein the hemostatic hydrogel composition comprises no greater than about 0.65 mole fraction of a fifth monomer of formula (VIII)


71. A method of preparing a hemostatic hydrogel composition comprising contacting an acrylated chitosan composition of any one of claims 1-11 with an oxidized dextran composition of any one of claims 33-45 thereby to produce the hemostatic hydrogel composition.
 72. The method of claim 71, wherein the ratio of the viscosity of the acrylated chitosan composition to the oxidized dextran composition ranges from about 100:1 to about 10,000:1.
 73. The method of claim 71, wherein the resulting hemostatic hydrogel composition is the hemostatic hydrogel composition of any one of claims 56-72.
 74. The method of any one of claims 71-73, wherein the hemostatic hydrogel composition further comprises a therapeutic agent.
 75. The method of any one of claims 71-74, wherein the hemostatic hydrogel composition further comprises a plurality of stem cells.
 76. The method of any one of claims 71-75, wherein the contacting the acrylated chitosan composition with the oxidized dextran composition is performed in a static mixer.
 77. The method of any one of claims 71-76, further comprising aerosolizing the mixture prior to application to tissue.
 78. The method of any one of claims 71-77, wherein the gelation time of the hemostatic hydrogel composition is less than 30 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition.
 79. The method of any one of claims 71-77, wherein the gelation time of the hemostatic hydrogel composition is within from about 10 seconds to about 240 seconds after contacting the acrylated chitosan composition with the oxidized dextran composition.
 80. A method of reducing or stopping blood loss at a location in a subject in need thereof, the method comprising forming at the location in the subject the hemostatic hydrogel composition of any one of claims 56-70 thereby to reduce or stop blood loss at the location.
 81. The method of claim 80, wherein the hemostatic hydrogel composition adheres to a tissue surface at the location.
 82. The method of claim 80 or 81, wherein platelets and/or red blood cells present at the location adhere to surfaces of pores in the hemostatic hydrogel composition.
 83. The method of any one of claims 80-82, wherein the hemostatic hydrogel composition promotes platelet adhesion and collection, platelet activation, and platelet aggregation and concentration at the location.
 84. The method of any one of claims 80-83, wherein the hemostatic hydrogel composition promotes a blood coagulation cascade to occur at the location.
 85. The method of any one of claims 80-84, wherein the hemostatic hydrogel composition promotes blood clot formation at the location.
 86. The method of any one of claims 80-85, wherein the blood loss is caused by trauma, abrasion, or surgical intervention at the location.
 87. The method of claim 86, wherein the surgical intervention is cardiac surgery, cranial surgery, spinal surgery, OB-GYN surgery, organ surgery, plastic surgery, a sinus procedure, thoracic surgery, a vascular surgery, a minimally invasive procedure, an arthroscopic procedure, an endoscopic procedure or a laparoscopic procedure.
 88. The method of claim 86 or 87, wherein the hemostatic hydrogel composition, when applied to the location, is capable of filling a cavity at the location without inducing compression of tissue surrounding the cavity when the hemostatic hydrogel composition is exposed to physiological fluid or a body fluid.
 89. The method of any one of claims 80-88, the method further comprising administering a therapeutic agent to the location.
 90. The method of claim 89, wherein the hemostatic hydrogel composition comprises the therapeutic agent.
 91. The method of any one of claims 80-88, the method further comprising administering a plurality of stem cells to the location.
 92. The method of claim 91, wherein the hemostatic hydrogel composition comprises the plurality of stem cells.
 93. The method of any one of claims 80-92, wherein hemostasis is achieved from about 5 seconds to about 120 seconds, from about 10 seconds to about 120 seconds, from about 15 seconds to about 120 seconds, from about 5 seconds to about 60 seconds, from about 10 seconds to about 60 seconds, from about 15 seconds to about 60 seconds, from about 5 seconds to about 30 seconds, from about 10 seconds to about 30 seconds, from about 15 seconds to about 30 seconds, from about 5 seconds to about 15 seconds, or from about 10 seconds to about 15 seconds, after the hemostatic hydrogel composition is applied to the location.
 94. The method of any one of claims 80-93, further comprising removing the hemostatic hydrogel composition from the subject after hemostasis.
 95. The method of claim 94, wherein the hemostatic hydrogel composition is removed by exposing the hemostatic hydrogel composition to a dissolution agent.
 96. The method of claim 95, wherein the dissolution agent is an organic compound comprising a primary amine and capable of breaking Schiff base linkages.
 97. A method of achieving hemostasis at a location in a subject in need thereof, the method comprising: (i) forming at the location in the subject the hemostatic hydrogel composition of any one of claims 56-70 to facilitate hemostasis; and (ii) removing the hemostatic hydrogel composition from the subject after hemostasis.
 98. The method of claim 97, wherein the hemostatic hydrogel composition adheres to a tissue surface at the location.
 99. The method of claim 97 or 98, wherein platelets and/or red blood cells present at the location adhere to surfaces of pores in the hemostatic hydrogel composition.
 100. The method of any one of claims 97-99, wherein the hemostatic hydrogel composition promotes platelet adhesion and collection, platelet activation, and platelet aggregation and concentration at the location.
 101. The method of any one of claims 97-100, wherein the hemostatic hydrogel composition promotes a blood coagulation cascade to occur at the location.
 102. The method of any one of claims 97-101, wherein the hemostatic hydrogel composition promotes blood clot formation at the location.
 103. The method of any one of claims 97-102, wherein the blood loss is caused by trauma, abrasion, or surgical intervention at the location.
 104. The method of any one of claims 97-103, wherein the hemostatic hydrogel composition is removed by exposing the hemostatic hydrogel composition to a dissolution agent.
 105. The method of any one of claims 97-104, wherein the dissolution agent is an organic compound comprising a primary amine and capable of breaking Schiff base linkages. 